A. Martyn Ainsworth
Royal Botanic Gardens
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by A. Martyn Ainsworth.
Fungal Diversity | 2014
D. Jean Lodge; Mahajabeen Padamsee; P. Brandon Matheny; M. Catherine Aime; Sharon A. Cantrell; David Boertmann; Alexander E. Kovalenko; Alfredo Vizzini; Bryn T. M. Dentinger; Paul M. Kirk; A. Martyn Ainsworth; Jean-Marc Moncalvo; Rytas Vilgalys; Ellen Larsson; Robert Lücking; Gareth W. Griffith; Matthew E. Smith; Lorelei L. Norvell; Dennis E. Desjardin; Scott A. Redhead; Clark L. Ovrebo; Edgar B. Lickey; Enrico Ercole; Karen W. Hughes; Régis Courtecuisse; Anthony Young; Manfred Binder; Andrew M. Minnis; Daniel L. Lindner; Beatriz Ortiz-Santana
Molecular phylogenies using 1–4 gene regions and information on ecology, morphology and pigment chemistry were used in a partial revision of the agaric family Hygro- phoraceae. The phylogenetically supported genera we recognize here in the Hygrophoraceae based on these and previous analyses are: Acantholichen, Ampulloclitocybe, Arrhenia, Cantharellula, Cantharocybe, Chromosera, Chrysomphalina, Cora, Corella, Cuphophyllus, Cyphellostereum, Dictyonema, Eonema, Gliophorus, Haasiella, Humidicutis, Hygroaster, Hygrocybe, Hygrophorus, Lichenomphalia, Neohygrocybe, Porpolomopsis and Pseudoarmillariella. A new genus that is sister to Chromosera is described as Gloioxanthomyces. Revisions were made at the ranks of subfamily, tribe, genus, subgenus, section and subsection. We present three new subfamilies, eight tribes (five new), eight subgenera (one new, one new combination and one stat. nov.), 26 sections (five new and three new combinations and two stat. nov.) and 14 subsections (two new, two stat. nov.). Species of Chromosera, Gliophorus, Humidicutis, and Neohygrocybe are often treated within the genus Hygrocybe; we therefore provide valid names in both classification systems. We used a minimalist approach in transferring genera and creating new names and combinations. Consequently, we retain in the Hygrophoraceae the basal cuphophylloid grade comprising the genera Cuphophyllus, Ampulloclitocybe and Cantharocybe, despite weak phylogenetic support. We include Aeruginospora and Semiomphalina in Hygrophoraceae based on morphology though molecular data are lacking. The lower hygrophoroid clade is basal to Hygrophoraceae s.s., comprising the genera Aphroditeola, Macrotyphula, Phyllotopsis, Pleurocybella, Sarcomyxa, Tricholomopsis and Typhula.
Lichenologist | 2014
David L. Hawksworth; Begoña Aguirre-Hudson; A. Martyn Ainsworth
The original material of Sphinctrina tigillaris, collected in 1864, was relocated, re-examined, found to represent a species of Chaenothecopsis , and is transferred to that genus as C. tigillaris comb. nov. It occurred on a specimen of a polypore, now identified as Perenniporia meridionalis , on a beam in a Northamptonshire church, and does not appear to have been collected since. Perenniporia meridionalis is a predominantly central and southern European species which has not previously been recognized in the British Isles, although other English specimens have now been located in collections at Kew and referred to the related P. medulla-panis. The name Sphinctrina tigillaris had been overlooked since its original description in 1865, and is nomenclaturally distinct from Lichen tigillaris, the basionym of Cyphelium tigillare. Notes on five other calicioid fungi found on polypores, and a key to the six now known, are also included.
PLOS ONE | 2017
Julieth O. Sousa; Laura M. Suz; Miguel Angel Garcia; Donis S. Alfredo; Luana Mayra Nunes Conrado; Paulo Marinho; A. Martyn Ainsworth; Iuri Goulart Baseia; María P. Martín
Since the nineteenth century, Myriostoma has been regarded as a monotypic genus with a widespread distribution in north temperate and subtropical regions. However, on the basis of morphological characters and phylogenetic evidence of DNA sequences of the internal transcribed spacer (ITS) regions and the large subunit nuclear ribosomal RNA gene (LSU), four species are now delimited: M. areolatum comb. & stat. nov., M. calongei sp. nov., M. capillisporum comb. & stat. nov., and M. coliforme. Myriostoma coliforme is typified by selecting a lectotype (iconotype) and a modern sequenced collection as an epitype. The four species can be discriminated by a combination of morphological characters, such as stomatal form, endoperidial surface texture, and basidiospore size and ornamentation.
IMA Fungus | 2018
Ross Scambler; Tuula Niskanen; Boris Assyov; A. Martyn Ainsworth; Jean-Michel Bellanger; Michael Loizides; Pierre-Arthur Moreau; Paul M. Kirk; Kare Liimatainen
In this study, eight species of Chroogomphus are recognized from Europe: C. britannicus, C. aff. filiformis 1, C. fulmineus, C. cf. helveticus, C. mediterraneus, C. cf. purpurascens, C. rutilus, and C. subfulmineus. Different candidates for the application of the name C. rutilus are evaluated and the best fit to the description is selected; lecto- and epitypes are chosen to fix the name. Chroogomphus fulmineus and C. mediterraneus are also epitypified and a new species, C. subfulmineus, is described. The infrageneric classification is revised and a new subgenus Siccigomphus and three new sections, Confusi, Filiformes, and Fulminei are introduced. The former sections Chroogomphus and Floccigomphus are elevated to subgeneric level. Comparison of the ITS regions (nuc rDNA ITS1-5.8S-ITS2) of all species studied shows that there is a minimum interspecific difference of 1.5 %, with the exception of the two species belonging to sect. Fulminei which differ by a minimum of 0.9 %. Ecological specimen data indicate that species of Chroogomphus form basidiomes under members of Pinaceae, with a general preference for species of Pinus. Five European species have been recorded under Picea, while Abies and Larix have also been recorded as tree associates, although the detailed nutritional relationships of the genus, involving other suilloid fungi in particular, have yet to be fully clarified.
Fungal Ecology | 2011
Lynne Boddy; Martha E. Crockatt; A. Martyn Ainsworth
Fungal Biology | 2007
David Parfitt; A. Martyn Ainsworth; Deborah J. Simpson; Hilary Joan Rogers; Lynne Boddy
Fungal Ecology | 2017
Nerea Abrego; Morten Bondo Christensen; Claus Bässler; A. Martyn Ainsworth; Jacob Heilmann-Clausen
Fungal Ecology | 2010
A. Martyn Ainsworth; David Parfitt; Hilary Joan Rogers; Lynne Boddy
Fungal Ecology | 2010
Martha E. Crockatt; Alice Campbell; Leanne Allum; A. Martyn Ainsworth; Lynne Boddy
Field Mycology | 2014
A. Martyn Ainsworth