A

Exidia candida Lloyd

Abstract

Exidia candida Lloyd, Mycological Writings 5: 620, 1916 Fig. 16 D, E = Exidia villosa Neuhoff, Pilze Mitteleuropas 2: 22, 1935. Neotype (designated by Spirin et al. 2018: 5). Norway. Oslo: Bygdøy, Dronningberget, Tilia cordata, 3 May 2016, Spirin 10012 * (O, studied). = Exidia cartilaginea S. Lundell & Neuhoff, Pilze Mitteleuropas 2: 19, 1935. Lectotype (selected by Spirin et al. 2018: 7). Sweden. Uppland: Bondkyrka, Vårdsätra, Betula sp., 18 Oct 1932, Lundell (Fungi Exsiccati Suecici # 263) (UPS F-010986, studied). Lectotype (selected by Spirin et al. 2018: 5). USA • Washington: Clallam Co., Sequim, [no collecting date], Grant (BPI 701884, studied) (Fig. 16 D, E). Description. Basidiomata annual, at first cushion-shaped or adpressed-orbicular, up to 5 cm in diam., broadly attached, later partly fusing together and forming compound cerebriform basidiomata, up to 20 cm in the longest dimension and 2 cm thick, gelatinous. Hymenial surface uneven or folded, occasionally bearing regularly arranged spine-like projections up to 0.3 mm long, white to cream-coloured or pale ochraceous-brownish, sometimes darker, reddish-brown, in dry condition darkening to brown or brownish-black. Abhymenial surface smooth, concolourous with hymenial surface. Margin sharply delimited, elevated, concolourous with hymenial surface, or adnate, fimbriate, whitish and gradually thinning. Hyphal structure monomitic, hyphae clamped; context hyphae hyaline, thin-walled or with a distinct wall, interwoven, anastomosing, 0.5–5 μm in diam., subhymenial hyphae hyaline or yellowish, thin-walled or with a distinct wall, predominantly interwoven, 1.5–4 μm in diam., basidia-bearing hyphae 2–4 μm in diam., often showing a zigzag-like branching pattern. Hyphidia with a hyaline or yellowish, hyphoid or narrowly clavate stem, 2.5–6 μm in diam., and hyaline or yellowish apical branches, 1–2 μm in diam., forming a continuous layer up to 40 μm thick. Probasidia clavate or tapering, 10–22 × 4–7 μm. Basidia four-celled, predominantly embedded, ellipsoid-ovoid, occasionally distinctly tapering to the base, (12 –) 12.5–18 (– 21) × (7.8 –) 7.9–11.3 (– 11.4) μm (n = 30 / 3), sometimes obliquely septate, sterigmata up to 30 × 2–2.5 μm. Basidiospores narrowly to broadly cylindrical, distinctly curved, (8.7 –) 8.9–15.2 (– 15.6) × (3.1 –) 3.2–5.2 (– 5.3) μm (n = 240 / 8), L = 10.23–12.40, W = 3.97–4.55, Q = 2.35–3.12. Remarks. Exidia candida was described from the US North-West (Lloyd 1916) and recently reinstated by Spirin et al. (2018). Here we redescribe it based on a larger set of specimens from the northern hemisphere. The species is macroscopically very variable. Its darker-colored forms with a well-developed epihymenial membrane were assigned to var. cartilaginea (Spirin et al. 2018). This variety occurs mainly in the northern areas of Eurasia. The southern, “ typical ” variety (= E. villosa) is lighter-coloured, softer and it often (but not always!) bears sharp outgrowths on the hymenial surface. This feature, as well as its shorter and wider basidiospores help to separate E. candida from the superficially similar D. repanda. Phylogenetically, E. candida is more closely related to the effused Exidia spp. (E. delita, E. japonica, E. plumbescens) than to other members of the genus with reflexed basidiomata (Figs 1, 2).

Authors 13

  1. University of Helsinki · Finnish Museum of Natural History

    Affiliation as printed

    Finnish Museum of Natural History, University of Helsinki, PO Box 7, 00014 Helsinki, Finland

  2. Komarov Botanical Institute of the Russian Academy of Sciences

    Affiliation as printed

    Komarov Botanical Institute, Prof. Popova str. 2, 197022 St. Petersburg, Russia

  3. Universität Hamburg

    Affiliation as printed

    Organismic Botany and Mycology, Institute of Plant Science and Microbiology, Ohnhorststraße 18, 22609 Hamburg, Germany

  4. Naturalis Biodiversity Center

    Affiliation as printed

    Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, Netherlands

  5. Affiliation as printed

    Société Linnéenne de Lyon, 33 rue Bossuet, 69006 Lyon, France

  6. Affiliation as printed

    Österplana Skattegården 2, 53384 Hällekis, Sweden

  7. University of Copenhagen

    Affiliation as printed

    Globe Institute, Department of Biology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen Ø, Denmark

  8. University of Oslo

    Affiliation as printed

    Institute of Biological Sciences, University of Oslo, P. O. Box 1045, Blindern, N- 0316 Oslo, Norway

  9. University of Tennessee at Knoxville

    Affiliation as printed

    Department of Ecology and Evolutionary Biology, University of Tennessee, 1406 Circle Drive, Knoxville, Tennessee 37996, USA

  10. University of Oulu

    Affiliation as printed

    Ecology and Genetics Research Unit, University of Oulu, P. O. Box 3000, FI- 90014 Oulu, Finland

  11. Czech Academy of Sciences, Biology Centre

    Affiliation as printed

    Biology Centre, Academy of Sciences of the Czech Republic, Branišovská 31, CZ 37005, České Budějovice, Czech Republic

  12. National University of Misiones

    Affiliation as printed

    Instituto de Biotecnología Misiones (InBioMis), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Ruta Nacional N 12, km 7.5, Posadas, Misiones, CP 3304, Argentina & Instituto Misionero de Biodiversidad (IMiBio), Ruta Nacional N 12, km 5, Puerto Iguazú, Misiones, CP 3370, Argentina

  13. University of Helsinki · Finnish Museum of Natural History

    Affiliation as printed

    Finnish Museum of Natural History, University of Helsinki, PO Box 7, 00014 Helsinki, Finland

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