Polypore (Aphyllophorales, Basidiomycetes) Studies in Russia
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Gymnosperms) of New York State
QK 129 . C667 1992 Pinophyta (Gymnosperms) of New York State Edward A. Cope The L. H. Bailey Hortorium Cornell University Contributions to a Flora of New York State IX Richard S. Mitchell, Editor 1992 Bulletin No. 483 New York State Museum The University of the State of New York THE STATE EDUCATION DEPARTMENT Albany, New York 12230 V A ThL U: ESTHER T. SVIERTZ LIBRARY THI-: ?‘HW YORK BOTANICAL GARDEN THE LuESTHER T. MERTZ LIBRARY THE NEW YORK BOTANICAL GARDEN Pinophyta (Gymnosperms) of New York State Edward A. Cope The L. H. Bailey Hortorium Cornell University Contributions to a Flora of New York State IX Richard S. Mitchell, Editor 1992 Bulletin No. 483 New York State Museum The University of the State of New York THE STATE EDUC ATION DEPARTMENT Albany, New York 12230 THE UNIVERSITY OF THE STATE OF NEW YORK Regents of The University Martin C. Barell, Chancellor, B.A., I.A., LL.B. Muttontown R. Carlos Carballada, Vice Chancellor, B.S. Rochester Willard A. Genrich, LL.B. Buffalo Emlyn I. Griffith. A.B.. J.D. Rome Jorge L. Batista, B.A.. J.D. Bronx Laura Bradley Chodos, B.A., M.A. Vischer Ferry Louise P. Matteoni, B.A., M.A., Ph.D. Bayside J. Edward Meyer, B.A., LL.B. Chappaqua FloydS. Linton, A.B., M.A., M.P.A. Miller Place Mimi Levin Lif.ber, B.A., M.A. Manhattan Shirley C. Brown, B.A., M.A., Ph.D. Albany Norma Gluck, B.A., M.S.W. Manhattan Adelaide L. Sanford, B.A., M.A., P.D. -
A New Species of Antrodia (Basidiomycota, Polypores) from China
Mycosphere 8(7): 878–885 (2017) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/8/7/4 Copyright © Guizhou Academy of Agricultural Sciences A new species of Antrodia (Basidiomycota, Polypores) from China Chen YY, Wu F* Institute of Microbiology, Beijing Forestry University, Beijing 100083, China Chen YY, Wu F 2017 –A new species of Antrodia (Basidiomycota, Polypores) from China. Mycosphere 8(7), 878–885, Doi 10.5943/mycosphere/8/7/4 Abstract A new species, Antrodia monomitica sp. nov., is described and illustrated from China based on morphological characters and molecular evidence. It is characterized by producing annual, fragile and nodulose basidiomata, a monomitic hyphal system with clamp connections on generative hyphae, hyaline, thin-walled and fusiform to mango-shaped basidiospores (6–7.5 × 2.3– 3 µm), and causing a typical brown rot. In phylogenetic analysis inferred from ITS and nLSU rDNA sequences, the new species forms a distinct lineage in the Antrodia s. l., and has a close relationship with A. oleracea. Key words – Fomitopsidaceae – phylogenetic analysis – taxonomy – wood-decaying fungi Introduction Antrodia P. Karst., typified with Polyporus serpens Fr. (=Antrodia albida (Fr.) Donk (Donk 1960, Ryvarden 1991), is characterized by a resupinate to effused-reflexed growth habit, white or pale colour of the context, a dimitic hyphal system with clamp connections on generative hyphae, hyaline, thin-walled, cylindrical to very narrow ellipsoid basidiospores which are negative in Melzer’s reagent and Cotton Blue, and causing a brown rot (Ryvarden & Melo 2014). Antrodia is a highly heterogeneous genus which is closely related to Fomitopsis P. -
Three Species of Wood-Decaying Fungi in <I>Polyporales</I> New to China
MYCOTAXON ISSN (print) 0093-4666 (online) 2154-8889 Mycotaxon, Ltd. ©2017 January–March 2017—Volume 132, pp. 29–42 http://dx.doi.org/10.5248/132.29 Three species of wood-decaying fungi in Polyporales new to China Chang-lin Zhaoa, Shi-liang Liua, Guang-juan Ren, Xiao-hong Ji & Shuanghui He* Institute of Microbiology, Beijing Forestry University, No. 35 Qinghuadong Road, Haidian District, Beijing 100083, P.R. China * Correspondence to: [email protected] Abstract—Three wood-decaying fungi, Ceriporiopsis lagerheimii, Sebipora aquosa, and Tyromyces xuchilensis, are newly recorded in China. The identifications were based on morphological and molecular evidence. The phylogenetic tree inferred from ITS+nLSU sequences of 49 species of Polyporales nests C. lagerheimii within the phlebioid clade, S. aquosa within the gelatoporia clade, and T. xuchilensis within the residual polyporoid clade. The three species are described and illustrated based on Chinese material. Key words—Basidiomycota, polypore, taxonomy, white rot fungus Introduction Wood-decaying fungi play a key role in recycling nutrients of forest ecosystems by decomposing cellulose, hemicellulose, and lignin of the plant cell walls (Floudas et al. 2015). Polyporales, a large order in Basidiomycota, includes many important genera of wood-decaying fungi. Recent molecular studies employing multi-gene datasets have helped to provide a phylogenetic overview of Polyporales, in which thirty-four valid families are now recognized (Binder et al. 2013). The diversity of wood-decaying fungi is very high in China because of the large landscape ranging from boreal to tropical zones. More than 1200 species of wood-decaying fungi have been found in China (Dai 2011, 2012), and some a Chang-lin Zhao and Shi-liang Liu contributed equally to this work and share first-author status 30 .. -
A Phylogenetic Overview of the Antrodia Clade (Basidiomycota, Polyporales)
Mycologia, 105(6), 2013, pp. 1391–1411. DOI: 10.3852/13-051 # 2013 by The Mycological Society of America, Lawrence, KS 66044-8897 A phylogenetic overview of the antrodia clade (Basidiomycota, Polyporales) Beatriz Ortiz-Santana1 phylogenetic studies also have recognized the genera Daniel L. Lindner Amylocystis, Dacryobolus, Melanoporia, Pycnoporellus, US Forest Service, Northern Research Station, Center for Sarcoporia and Wolfiporia as part of the antrodia clade Forest Mycology Research, One Gifford Pinchot Drive, (SY Kim and Jung 2000, 2001; Binder and Hibbett Madison, Wisconsin 53726 2002; Hibbett and Binder 2002; SY Kim et al. 2003; Otto Miettinen Binder et al. 2005), while the genera Antrodia, Botanical Museum, University of Helsinki, PO Box 7, Daedalea, Fomitopsis, Laetiporus and Sparassis have 00014, Helsinki, Finland received attention in regard to species delimitation (SY Kim et al. 2001, 2003; KM Kim et al. 2005, 2007; Alfredo Justo Desjardin et al. 2004; Wang et al. 2004; Wu et al. 2004; David S. Hibbett Dai et al. 2006; Blanco-Dios et al. 2006; Chiu 2007; Clark University, Biology Department, 950 Main Street, Worcester, Massachusetts 01610 Lindner and Banik 2008; Yu et al. 2010; Banik et al. 2010, 2012; Garcia-Sandoval et al. 2011; Lindner et al. 2011; Rajchenberg et al. 2011; Zhou and Wei 2012; Abstract: Phylogenetic relationships among mem- Bernicchia et al. 2012; Spirin et al. 2012, 2013). These bers of the antrodia clade were investigated with studies also established that some of the genera are molecular data from two nuclear ribosomal DNA not monophyletic and several modifications have regions, LSU and ITS. A total of 123 species been proposed: the segregation of Antrodia s.l. -
Chapter 10 • Principles of Conserving the Arctic's Biodiversity
Chapter 10 Principles of Conserving the Arctic’s Biodiversity Lead Author Michael B. Usher Contributing Authors Terry V.Callaghan, Grant Gilchrist, Bill Heal, Glenn P.Juday, Harald Loeng, Magdalena A. K. Muir, Pål Prestrud Contents Summary . .540 10.1. Introduction . .540 10.2. Conservation of arctic ecosystems and species . .543 10.2.1. Marine environments . .544 10.2.2. Freshwater environments . .546 10.2.3. Environments north of the treeline . .548 10.2.4. Boreal forest environments . .551 10.2.5. Human-modified habitats . .554 10.2.6. Conservation of arctic species . .556 10.2.7. Incorporating traditional knowledge . .558 10.2.8. Implications for biodiversity conservation . .559 10.3. Human impacts on the biodiversity of the Arctic . .560 10.3.1. Exploitation of populations . .560 10.3.2. Management of land and water . .562 10.3.3. Pollution . .564 10.3.4. Development pressures . .566 10.4. Effects of climate change on the biodiversity of the Arctic . .567 10.4.1. Changes in distribution ranges . .568 10.4.2. Changes in the extent of arctic habitats . .570 10.4.3. Changes in the abundance of arctic species . .571 10.4.4. Changes in genetic diversity . .572 10.4.5. Effects on migratory species and their management . .574 10.4.6. Effects caused by non-native species and their management .575 10.4.7. Effects on the management of protected areas . .577 10.4.8. Conserving the Arctic’s changing biodiversity . .579 10.5. Managing biodiversity conservation in a changing environment . .579 10.5.1. Documenting the current biodiversity . .580 10.5.2. -
Relationships Between Wood-Inhabiting Fungal Species
Silva Fennica 45(5) research articles SILVA FENNICA www.metla.fi/silvafennica · ISSN 0037-5330 The Finnish Society of Forest Science · The Finnish Forest Research Institute Relationships between Wood-Inhabiting Fungal Species Richness and Habitat Variables in Old-Growth Forest Stands in the Pallas-Yllästunturi National Park, Northern Boreal Finland Inari Ylläsjärvi, Håkan Berglund and Timo Kuuluvainen Ylläsjärvi, I., Berglund, H. & Kuuluvainen, T. 2011. Relationships between wood-inhabiting fungal species richness and habitat variables in old-growth forest stands in the Pallas-Yllästunturi National Park, northern boreal Finland. Silva Fennica 45(5): 995–1013. Indicators for biodiversity are needed for efficient prioritization of forests selected for conservation. We analyzed the relationships between 86 wood-inhabiting fungal (polypore) species richness and 35 habitat variables in 81 northern boreal old-growth forest stands in Finland. Species richness and the number of red-listed species were analyzed separately using generalized linear models. Most species were infrequent in the studied landscape and no species was encountered in all stands. The species richness increased with 1) the volume of coarse woody debris (CWD), 2) the mean DBH of CWD and 3) the basal area of living trees. The number of red-listed species increased along the same gradients, but the effect of basal area was not significant. Polypore species richness was significantly lower on western slopes than on flat topography. On average, species richness was higher on northern and eastern slopes than on western and southern slopes. The results suggest that a combination of habitat variables used as indicators may be useful in selecting forest stands to be set aside for polypore species conservation. -
Ten Principles for Conservation Translocations of Threatened Wood- Inhabiting Fungi
Ten principles for conservation translocations of threatened wood- inhabiting fungi Jenni Nordén 1, Nerea Abrego 2, Lynne Boddy 3, Claus Bässler 4,5 , Anders Dahlberg 6, Panu Halme 7,8 , Maria Hällfors 9, Sundy Maurice 10 , Audrius Menkis 6, Otto Miettinen 11 , Raisa Mäkipää 12 , Otso Ovaskainen 9,13 , Reijo Penttilä 12 , Sonja Saine 9, Tord Snäll 14 , Kaisa Junninen 15,16 1Norwegian Institute for Nature Research, Gaustadalléen 21, NO-0349 Oslo, Norway. 2Dept of Agricultural Sciences, P.O. Box 27, FI-00014 University of Helsinki, Finland. 3Cardiff School of Biosciences, Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, UK 4Bavarian Forest National Park, D-94481 Grafenau, Germany. 5Technical University of Munich, Chair for Terrestrial Ecology, D-85354 Freising, Germany. 6Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, P.O.Box 7026, 750 07 Uppsala, Sweden. 7Department of Biological and Environmental Science, P.O. Box 35, FI-40014 University of Jyväskylä, Finland. 8School of Resource Wisdom, P.O. Box 35, FI-40014 University of Jyväskylä, Finland. 9Organismal and Evolutionary Biology Research Programme, P.O. Box 65, FI-00014 University of Helsinki, Finland. 10 Section for Genetics and Evolutionary Biology, University of Oslo, Blindernveien 31, 0316 Oslo, Norway. 11 Finnish Museum of Natural History, P.O. Box 7, FI-00014 University of Helsinki, Finland. 12 Natural Resources Institute Finland (Luke), Latokartanonkaari 9, FI-00790 Helsinki, Finland. 13 Centre for Biodiversity Dynamics, Department of Biology, Norwegian University of Science and Technology, N-7491 Trondheim, Norway. 14 Artdatabanken, Swedish University of Agricultural Sciences, P.O. Box 7007, SE-75007 Uppsala, Sweden. -
Polypore Diversity in North America with an Annotated Checklist
Mycol Progress (2016) 15:771–790 DOI 10.1007/s11557-016-1207-7 ORIGINAL ARTICLE Polypore diversity in North America with an annotated checklist Li-Wei Zhou1 & Karen K. Nakasone2 & Harold H. Burdsall Jr.2 & James Ginns3 & Josef Vlasák4 & Otto Miettinen5 & Viacheslav Spirin5 & Tuomo Niemelä 5 & Hai-Sheng Yuan1 & Shuang-Hui He6 & Bao-Kai Cui6 & Jia-Hui Xing6 & Yu-Cheng Dai6 Received: 20 May 2016 /Accepted: 9 June 2016 /Published online: 30 June 2016 # German Mycological Society and Springer-Verlag Berlin Heidelberg 2016 Abstract Profound changes to the taxonomy and classifica- 11 orders, while six other species from three genera have tion of polypores have occurred since the advent of molecular uncertain taxonomic position at the order level. Three orders, phylogenetics in the 1990s. The last major monograph of viz. Polyporales, Hymenochaetales and Russulales, accom- North American polypores was published by Gilbertson and modate most of polypore species (93.7 %) and genera Ryvarden in 1986–1987. In the intervening 30 years, new (88.8 %). We hope that this updated checklist will inspire species, new combinations, and new records of polypores future studies in the polypore mycota of North America and were reported from North America. As a result, an updated contribute to the diversity and systematics of polypores checklist of North American polypores is needed to reflect the worldwide. polypore diversity in there. We recognize 492 species of polypores from 146 genera in North America. Of these, 232 Keywords Basidiomycota . Phylogeny . Taxonomy . species are unchanged from Gilbertson and Ryvarden’smono- Wood-decaying fungus graph, and 175 species required name or authority changes. -
Bold Park Fungi Report
Client report to the Botanic Gardens and Parks Authority Fungi survey - Bold Park 2009 Author: N. L. Bougher Department of Environment and C onservation, Western Australia December 2009 In conjunction with the Perth Urban Bushland Fungi Project ____________________________________________________________ Fungi Survey Bold Park 2009 © N. L. Bougher Department of Environment & Conservation 2009 1 of 24 Figures 1 - 4: Examples of the new records of fungi discovered in Bold Park during 2009. Each of these species is highlighted in the discussion section of this report. Figure 1: Martininia panamaensis (E9411) (Top) fruit bodies. (Bottom) sclerotia extracted from a Macrozamia frond. Figure 2: Gymnogaster boletoides (BOUGHER 528) Figure 4: Mycena tenerrima (E9444) Figure 3: Chondrogaster sp. (E9397) (Top) Mass of chewing gum mycelium. (Bottom) Sectioned fruit body. ____________________________________________________________ Fungi Survey Bold Park 2009 © N. L. Bougher Department of Environment & Conservation 2009 2 of 24 Figures 5 - 8: Examples of the new records of fungi discovered in Bold Park during 2009. Each of these species is highlighted in the discussion section of this report. Figure 5: Xerula gigaspora (E9375) Figure 6: Coprinellus angulatus Top (E9470). Bottom (E9473) sterile, albino fruit bodies (left), and normally pigmented fruit body (right) Figure 7: Skeletocutis amorpha (BOUGHER538) Figure 8: Hyphoderma assimile (E9472) ____________________________________________________________ Fungi Survey Bold Park 2009 © N. L. Bougher Department of Environment & Conservation 2009 3 of 24 Fungi Survey - Bold Park 2009 Background and Objectives Bold Park is a regionally significant bushland located in the west metropolitan area of Perth, Western Australia. The park incorporates more than 400 hectares of diverse vegetation types on Spearwood and Quindalup dune systems such as eucalypt and banksias woodlands, acacia shrublands, and coastal and limestone heath ((Keighery et al., 1990; Barrett and Tay, 2005). -
Wood-Decaying Basidiomycetes Associated with Dwarf Siberian Pine in Northeast Siberia and the Kamchatka Peninsula
Wood-decaying Basidiomycetes Associated with Dwarf Siberian Pine in Northeast Siberia and the Kamchatka Peninsula Mukhin, V. A.; Knudsen, H.; Kotiranta, H.; Corfixen, P.; Kostitsina, M. V. Publication date: 2018 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Mukhin, V. A., Knudsen, H., Kotiranta, H., Corfixen, P., & Kostitsina, M. V. (2018). Wood-decaying Basidiomycetes Associated with Dwarf Siberian Pine in Northeast Siberia and the Kamchatka Peninsula. 125- 133. Paper presented at The Fourth International Scientific Conference Ecology and Geography of Plants and Plant Communities, Ekaterinburg, Russian Federation. https://knepublishing.com/index.php/KnE- Life/article/view/3230 Download date: 29. Sep. 2021 Ecology and Geography of Plants and Plant Communities The fourth International Scientific Conference on Ecology and Geography of Plants and Plant Communities Volume 2018 Conference Paper Wood-decaying Basidiomycetes Associated with Dwarf Siberian Pine in Northeast Siberia and the Kamchatka Peninsula V. A. Mukhin1,2, H. Knudsen3, H. Kotiranta4, P. Corfixen3, and M. V. Kostitsina2 1Institute of the Natural Sciences and Mathematics, Ural Federal University, 620002 Ekaterin- burg, Russia 2Institute of Plant and Animal Ecology, Ural Branch of the Russian Academy of Sciences, 620144 Ekaterinburg, Russia 3Natural History Museum of Denmark, University of Copenhagen, DK–1323, Copenhagen K, Denmark 4Finnish Environment Institute, FI–00251, Helsinki, Finland Abstract A survey of the biodiversity of wood-decaying Basidiomycetes associated with Pinus pumila (the dwarf Siberian pine), a highly characteristic woody plant of Northeast Corresponding Author: Siberia and the Kamchatka Peninsula, is presented for the first time. Thirty-two V. -
Polypore Fungi As a Flagship Group to Indicate Changes in Biodiversity – a Test Case from Estonia Kadri Runnel1* , Otto Miettinen2 and Asko Lõhmus1
Runnel et al. IMA Fungus (2021) 12:2 https://doi.org/10.1186/s43008-020-00050-y IMA Fungus RESEARCH Open Access Polypore fungi as a flagship group to indicate changes in biodiversity – a test case from Estonia Kadri Runnel1* , Otto Miettinen2 and Asko Lõhmus1 Abstract Polyporous fungi, a morphologically delineated group of Agaricomycetes (Basidiomycota), are considered well studied in Europe and used as model group in ecological studies and for conservation. Such broad interest, including widespread sampling and DNA based taxonomic revisions, is rapidly transforming our basic understanding of polypore diversity and natural history. We integrated over 40,000 historical and modern records of polypores in Estonia (hemiboreal Europe), revealing 227 species, and including Polyporus submelanopus and P. ulleungus as novelties for Europe. Taxonomic and conservation problems were distinguished for 13 unresolved subgroups. The estimated species pool exceeds 260 species in Estonia, including at least 20 likely undescribed species (here documented as distinct DNA lineages related to accepted species in, e.g., Ceriporia, Coltricia, Physisporinus, Sidera and Sistotrema). Four broad ecological patterns are described: (1) polypore assemblage organization in natural forests follows major soil and tree-composition gradients; (2) landscape-scale polypore diversity homogenizes due to draining of peatland forests and reduction of nemoral broad-leaved trees (wooded meadows and parks buffer the latter); (3) species having parasitic or brown-rot life-strategies are more substrate- specific; and (4) assemblage differences among woody substrates reveal habitat management priorities. Our update reveals extensive overlap of polypore biota throughout North Europe. We estimate that in Estonia, the biota experienced ca. 3–5% species turnover during the twentieth century, but exotic species remain rare and have not attained key functions in natural ecosystems. -
3. Overview of Existing Fungus Monitoring Protocols
Version 2.9, 20.12.2004 Monitoring protocol for wood-inhabiting fungi in the Alberta Biodiversity Monitoring Program for the Alberta Biodiversity Monitoring Program Jogeir N. Stokland 1 Anna-Liisa Sippola 2 December 2004 1Norwegian Institute of Land Inventory, Norway 2University of Lapland, Arctic Centre, Finland 1 Disclaimer The views, statements, and conclusions expressed in this report are those of the authors and should not be construed as conclusions or opinions of the ABMP. Development of the ABMP has continued since this report was produced. Thus, the report may not accurately reflect current ideas. 2 1. INTRODUCTION ...................................................................................................................... 4 1.1 Brief introduction to biodiversity in dead wood................................................................... 4 1.2 Knowledge about fungus diversity in Alberta and Canada .................................................. 5 2. FUNGAL DIVERSITY ON DEAD WOOD IN BOREAL FORESTS...................................... 5 2.1. Different fungus groups - their strengths and weaknesses for long-term monitoring ......... 5 2.2 Dead wood attributes that are important to fungal diversity............................................... 12 2.3 Brief comparison of fungi on dead wood in Scandinavia and Canada............................... 14 2.4 Brief description of Alberta forest types and expected fungus diversity patterns .............. 15 2.5 Polypore species diversity at local and regional levels......................................................