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Chorioactidaceae: a New Family in the Pezizales (Ascomycota) with Four Genera
mycological research 112 (2008) 513–527 journal homepage: www.elsevier.com/locate/mycres Chorioactidaceae: a new family in the Pezizales (Ascomycota) with four genera Donald H. PFISTER*, Caroline SLATER, Karen HANSENy Harvard University Herbaria – Farlow Herbarium of Cryptogamic Botany, Department of Organismic and Evolutionary Biology, Harvard University, 22 Divinity Avenue, Cambridge, MA 02138, USA article info abstract Article history: Molecular phylogenetic and comparative morphological studies provide evidence for the Received 15 June 2007 recognition of a new family, Chorioactidaceae, in the Pezizales. Four genera are placed in Received in revised form the family: Chorioactis, Desmazierella, Neournula, and Wolfina. Based on parsimony, like- 1 November 2007 lihood, and Bayesian analyses of LSU, SSU, and RPB2 sequence data, Chorioactidaceae repre- Accepted 29 November 2007 sents a sister clade to the Sarcosomataceae, to which some of these taxa were previously Corresponding Editor: referred. Morphologically these genera are similar in pigmentation, excipular construction, H. Thorsten Lumbsch and asci, which mostly have terminal opercula and rounded, sometimes forked, bases without croziers. Ascospores have cyanophilic walls or cyanophilic surface ornamentation Keywords: in the form of ridges or warts. So far as is known the ascospores and the cells of the LSU paraphyses of all species are multinucleate. The six species recognized in these four genera RPB2 all have limited geographical distributions in the northern hemisphere. Sarcoscyphaceae ª 2007 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Sarcosomataceae SSU Introduction indicated a relationship of these taxa to the Sarcosomataceae and discussed the group as the Chorioactis clade. Only six spe- The Pezizales, operculate cup-fungi, have been put on rela- cies are assigned to these genera, most of which are infre- tively stable phylogenetic footing as summarized by Hansen quently collected. -
Diversity and Phylogeny of Suillus (Suillaceae; Boletales; Basidiomycota) from Coniferous Forests of Pakistan
INTERNATIONAL JOURNAL OF AGRICULTURE & BIOLOGY ISSN Print: 1560–8530; ISSN Online: 1814–9596 13–870/2014/16–3–489–497 http://www.fspublishers.org Full Length Article Diversity and Phylogeny of Suillus (Suillaceae; Boletales; Basidiomycota) from Coniferous Forests of Pakistan Samina Sarwar * and Abdul Nasir Khalid Department of Botany, University of the Punjab, Quaid-e-Azam Campus, Lahore, 54950, Pakistan *For correspondence: [email protected] Abstract Suillus (Boletales; Basidiomycota) is an ectomycorrhizal genus, generally associated with Pinaceae. Coniferous forests of Pakistan are rich in mycodiversity and Suillus species are found as early appearing fungi in the vicinity of conifers. This study reports the diversity of Suillus collected during a period of three (3) years (2008-2011). From 32 basidiomata of Suillus collected, 12 species of this genus were identified. These basidiomata were characterized morphologically, and phylogenetically by amplifying and sequencing the ITS region of rDNA. © 2014 Friends Science Publishers Keywords: Moist temperate forests; PCR; rDNA; Ectomycorrhizae Introduction adequate temperature make the environment suitable for the growth of mushrooms in these forests. Suillus (Suillaceae, Basidiomycota, Boletales ) forms This paper described the diversity of Suillus (Boletes, ectomycorrhizal associations mostly with members of the Fungi) with the help of the anatomical, morphological and Pinaceae and is characterized by having slimy caps, genetic analyses as little knowledge is available from forests glandular dots on the stipe, large pore openings that are in Pakistan. often arranged radially and a partial veil that leaves a ring or tissue hanging from the cap margin (Kuo, 2004). This genus Materials and Methods is mostly distributed in northern temperate locations, although some species have been reported in the southern Sporocarp Collection hemisphere as well (Kirk et al ., 2008). -
Project Cover Sheet
Rocky Mountains Cooperative Ecosystem Studies Unit (RM-CESU) RM-CESU Cooperative Agreement Number: H1200040001 PROJECT COVER SHEET TITLE OF PROJECT: Investigation of Mycorrhizal fungi associated with whitebark pine in Waterton Lakes- Glacier National Parks Ecosystem. NAME OF PARK/NPS UNIT: Glacier NP NAME OF UNIVERSITY PARTNER: Montana State University NPS KEY OFFICIAL: Joyce Lapp Glacier National Park West Glacier, MT 59936 406-888-7817 [email protected] PRINCIPAL INVESTIGATOR: Cathy L. Cripps Department of Plant Sciences & Plant Pathology 119 Plant BioSciences Building Montana State University Bozeman, MT 59717 [email protected] 406-994-5226 COST OF PROJECT: Direct Cost: $ 1000.00 Indirect Cost (CESU overhead): $ 175.00 Total Cost: $ 1,175.00 NPS ACCOUNT NUMBER: 1430-7077-634 NAME OF FUND SOURCE: IMR-IMRICO PROJECT SCHEDULE, FINAL PRODUCTS, AND PAYMENTS Date of Project Initiation: May 1, 2007 List of Products: (1) Field collection of ectomycorrhizae from Whitebark pine and identification of this fungi, (2) final report due on March 31, 2008. Payment Schedule: Invoices as received from the University. End Date of Project: May 1, 2008 1 GLACIER NATIONAL PARK Investigation of Native Mycorrhizal Fungi with Whitebark Pine Final Report 2009 Cathy Cripps, Montana State University ([email protected]) INTRODUCTION Whitebark pine is a picturesque, long-lived tree of high mountain landscapes in much of the American West. It is a "keystone” species supplying food and shelter for wildlife and often holding the snow and rocky soils in places where other trees cannot grow. Now, however, in about half of its natural range, including Waterton-Glacier NP, whitebark pine is mostly dead or dying, due to an introduced blister rust disease and replacement by competing trees as a result of fire exclusion (Schwandt 2006, Tomback & Kendall 2001, Kendrick & Keane 2001). -
Inoculation of Whitebark Pine Seedlings with Native Ectomycorrhizal Fungi
Inoculation of Whitebark Pine Seedlings with Native Ectomycorrhizal Fungi Cathy Cripps and Marlee Jenkins Montana State University, Bozeman MT Most ecosystems are predicated on the existence of microscopic fungi on the roots of plants (that form mycorrhizae) E.O. Wilson What are Ectomycorrhizal fungi? • mutualistic with tree roots Suillus fruiting body • promote phosphorus & nitrogen uptake in trees • protect tree roots (heavy metals, grazers, etc) • improve drought tolerance •improve tree health & seedling establishment Trees: Birch, Oak, Willow, Aspen, Eucalyptus, Alder, Pine, Spruce, Fir, Larch, Douglas fir All pines depend on ectomycorrhizal fungi to survive in nature (Read 1998) Can these native mycorrhizal FUNGI be used ectomycorrhizae as a tool in WHITEBARK PINE restoration? Read photo 1989 There are many kinds of Ectomycorrhizal fungi: which ones could be useful? 5,000-8,000 species of fungi • Each tree species hosts a particular set of mycorrhizal fungi • Each tree hosts a ‘community” of mycorrhizal fungi (many different species) • Each fungus provides unique benefits • Some ECM fungi are host specific Cripps, CL 2002. Mycorrhiza. In: Pscheidt & Ocamb, Pacfic NW Plant Disease Management Handbook. Austria has been inoculating European Stone Pine (Pinus cembra) seedlings for restoration for 50 years To stabilize slopes from avalanches Inoculation with ectomycorrhizal fungi: after trees were cut down for grazing Increased seedling survival from 50% to 90 % at high elevations Visit to Federal Institute Nursery Weisleitner Austrian -
A Preliminary Checklist of Arizona Macrofungi
A PRELIMINARY CHECKLIST OF ARIZONA MACROFUNGI Scott T. Bates School of Life Sciences Arizona State University PO Box 874601 Tempe, AZ 85287-4601 ABSTRACT A checklist of 1290 species of nonlichenized ascomycetaceous, basidiomycetaceous, and zygomycetaceous macrofungi is presented for the state of Arizona. The checklist was compiled from records of Arizona fungi in scientific publications or herbarium databases. Additional records were obtained from a physical search of herbarium specimens in the University of Arizona’s Robert L. Gilbertson Mycological Herbarium and of the author’s personal herbarium. This publication represents the first comprehensive checklist of macrofungi for Arizona. In all probability, the checklist is far from complete as new species await discovery and some of the species listed are in need of taxonomic revision. The data presented here serve as a baseline for future studies related to fungal biodiversity in Arizona and can contribute to state or national inventories of biota. INTRODUCTION Arizona is a state noted for the diversity of its biotic communities (Brown 1994). Boreal forests found at high altitudes, the ‘Sky Islands’ prevalent in the southern parts of the state, and ponderosa pine (Pinus ponderosa P.& C. Lawson) forests that are widespread in Arizona, all provide rich habitats that sustain numerous species of macrofungi. Even xeric biomes, such as desertscrub and semidesert- grasslands, support a unique mycota, which include rare species such as Itajahya galericulata A. Møller (Long & Stouffer 1943b, Fig. 2c). Although checklists for some groups of fungi present in the state have been published previously (e.g., Gilbertson & Budington 1970, Gilbertson et al. 1974, Gilbertson & Bigelow 1998, Fogel & States 2002), this checklist represents the first comprehensive listing of all macrofungi in the kingdom Eumycota (Fungi) that are known from Arizona. -
The Phylogeny of Plant and Animal Pathogens in the Ascomycota
Physiological and Molecular Plant Pathology (2001) 59, 165±187 doi:10.1006/pmpp.2001.0355, available online at http://www.idealibrary.com on MINI-REVIEW The phylogeny of plant and animal pathogens in the Ascomycota MARY L. BERBEE* Department of Botany, University of British Columbia, 6270 University Blvd, Vancouver, BC V6T 1Z4, Canada (Accepted for publication August 2001) What makes a fungus pathogenic? In this review, phylogenetic inference is used to speculate on the evolution of plant and animal pathogens in the fungal Phylum Ascomycota. A phylogeny is presented using 297 18S ribosomal DNA sequences from GenBank and it is shown that most known plant pathogens are concentrated in four classes in the Ascomycota. Animal pathogens are also concentrated, but in two ascomycete classes that contain few, if any, plant pathogens. Rather than appearing as a constant character of a class, the ability to cause disease in plants and animals was gained and lost repeatedly. The genes that code for some traits involved in pathogenicity or virulence have been cloned and characterized, and so the evolutionary relationships of a few of the genes for enzymes and toxins known to play roles in diseases were explored. In general, these genes are too narrowly distributed and too recent in origin to explain the broad patterns of origin of pathogens. Co-evolution could potentially be part of an explanation for phylogenetic patterns of pathogenesis. Robust phylogenies not only of the fungi, but also of host plants and animals are becoming available, allowing for critical analysis of the nature of co-evolutionary warfare. Host animals, particularly human hosts have had little obvious eect on fungal evolution and most cases of fungal disease in humans appear to represent an evolutionary dead end for the fungus. -
Morchella Exuberans – Ny Murkla För Sverige
Svensk Mykologisk Tidskrift Volym 36 · nummer 3 · 2015 Svensk Mykologisk Tidskrift 1J@C%RV`:` 1R1$:`7 www.svampar.se 0VJ@7@QCQ$1@/ Sveriges Mykologiska Förening /VJ]%GC1HV`:`Q`1$1J:C:` 1@C:`IVR0:I]R Föreningen verkar för :J@J7 J1J$QH.IVR0VJ@ QH.JQ`RV%`Q]V1@ R VJ G?`V @?JJVRQI QI 0V`1$V 0:I]:` QH. 1J `VV8/VJ% @QIIV`IVR`7`:J%IIV` 0:I]:``QCC1J: %`VJ ]V`B`QH.?$:00V`1$V7@QCQ$1@:DV`VJ1J$8 R@7RR:0J: %`VJQH.:0:I]]CQH@J1J$QH.- 9 `%@ 1QJV` 1CC`V``: :`V`1JJ]BD7.VI1R: J: %]] `?R:JRV1@Q$QH.I:`@@V`%JRV`1:@ - 11180:I]:`8V8/VJV`.BCC$VJQI- :$:JRV:0$?CC:JRVC:$:` CVI@:] 1 D8/VJ ``:I ?CC IVR G1R`:$ R : @QJ :@ V` IVCC:J CQ@:C: 0:I]`V`VJ1J$:` QH. ``BJ/Q`V<: .Q` I1JJV`QJR8 0:I]1J `VV`:RV1C:JRV %JRV`C?: R:@QJ :@ %]]`?.BCCIVRI7@QCQ$1@:`V`- $:`1$`:JJC?JRV` R VJ :I0V`@:J IVR I7@QCQ$1@ `Q`@J1J$ QH. Redaktion 0V VJ@:]8 JVR:@ V`QH.:J0:`1$% $10:`V 1@:VCKQJ VRCVI@:]V`.BCCV$VJQI1J?J1J$:0IVRCVIR LH=: :J :0 VJ]B`V`VJ1J$VJG:J@$1`Q /JNLLHO//;< 5388-7733 =0:I]:`8V VRCVI:0 VJ` 7 [ 7`V`IVRCVII:`GQ::10V`1$V H=AQJVGQ`$ [ 7`V`IVRCVII:`GQ::% :J`V`0V`1$V G:`J: :`0V [ 7 `V` %RV`:JRVIVRCVII:`GQ::1 6: .:II:`01@ 0V`1$^6 _ VC8 [ 7 `V``=^=/_ =8H`QJVGQ`QI %GH`1]``QI:G`Q:R:`V1VCHQIV82:7IVJ Jan Nilsson `Q` ^46 _H:JGVI:RVG7H`VR1 H:`RG7 IVGV`$ 01Q%`1VG.Q]: 11180:I]:`8VQ` QQ%` :LL;J4< G:J@:HHQ%J7 =$8V 9:;<74 :9AL9D/74E4 Äldre nummer :00VJ@7@QCQ$1@/^ KNJE/KOJ<;<_`1JJ]BVJAEQI@:JGV ?CC: Sveriges Mykologiska Förening ``BJD8 9=V VJ@:] Previous issues Q` 0VJ@ 7@QCQ$1@ / ^KNJE/KOJ<;<_:`V:0:1C:GCVQJ:AE1 GVGQ`$%J10V`1 V H:JGVQ`RV`VR``QID8 :6 GVGQ`$ 11180:I]:`8V Omslagsbild 2:]V$=:6^C1Q].Q`%]1:H1J%_DQ H_ 8 I detta nummer nr 3 2015 *_77`J`7 SMF 2 Kompakt taggsvamp (Hydnellum compac- B`0]%]IG$ tum_ŽJB$`: :J@:`QIRVV@. -
Suomen Helttasienten Ja Tattien Ekologia, Levinneisyys Ja Uhanalaisuus
Suomen ympäristö 769 LUONTO JA LUONNONVARAT Pertti Salo, Tuomo Niemelä, Ulla Nummela-Salo ja Esteri Ohenoja (toim.) Suomen helttasienten ja tattien ekologia, levinneisyys ja uhanalaisuus .......................... SUOMEN YMPÄRISTÖKESKUS Suomen ympäristö 769 Pertti Salo, Tuomo Niemelä, Ulla Nummela-Salo ja Esteri Ohenoja (toim.) Suomen helttasienten ja tattien ekologia, levinneisyys ja uhanalaisuus SUOMEN YMPÄRISTÖKESKUS Viittausohje Viitatessa tämän raportin lukuihin, käytetään lukujen otsikoita ja lukujen kirjoittajien nimiä: Esim. luku 5.2: Kytövuori, I., Nummela-Salo, U., Ohenoja, E., Salo, P. & Vauras, J. 2005: Helttasienten ja tattien levinneisyystaulukko. Julk.: Salo, P., Niemelä, T., Nummela-Salo, U. & Ohenoja, E. (toim.). Suomen helttasienten ja tattien ekologia, levin- neisyys ja uhanalaisuus. Suomen ympäristökeskus, Helsinki. Suomen ympäristö 769. Ss. 109-224. Recommended citation E.g. chapter 5.2: Kytövuori, I., Nummela-Salo, U., Ohenoja, E., Salo, P. & Vauras, J. 2005: Helttasienten ja tattien levinneisyystaulukko. Distribution table of agarics and boletes in Finland. Publ.: Salo, P., Niemelä, T., Nummela- Salo, U. & Ohenoja, E. (eds.). Suomen helttasienten ja tattien ekologia, levinneisyys ja uhanalaisuus. Suomen ympäristökeskus, Helsinki. Suomen ympäristö 769. Pp. 109-224. Julkaisu on saatavana myös Internetistä: www.ymparisto.fi/julkaisut ISBN 952-11-1996-9 (nid.) ISBN 952-11-1997-7 (PDF) ISSN 1238-7312 Kannen kuvat / Cover pictures Vasen ylä / Top left: Paljakkaa. Utsjoki. Treeless alpine tundra zone. Utsjoki. Kuva / Photo: Esteri Ohenoja Vasen ala / Down left: Jalopuulehtoa. Parainen, Lenholm. Quercus robur forest. Parainen, Lenholm. Kuva / Photo: Tuomo Niemelä Oikea ylä / Top right: Lehtolohisieni (Laccaria amethystina). Amethyst Deceiver (Laccaria amethystina). Kuva / Photo: Pertti Salo Oikea ala / Down right: Vanhaa metsää. Sodankylä, Luosto. Old virgin forest. Sodankylä, Luosto. Kuva / Photo: Tuomo Niemelä Takakansi / Back cover: Ukonsieni (Macrolepiota procera). -
Delivering Biodiversity Conservation an Initiative by SCA
Delivering biodiversity conservation An initiative by SCA March 2021 Contents Summary .................................................................................................................... 2 Background ................................................................................................................ 3 Introduction to SCA ................................................................................................. 3 What are we achieving with this initiative? .............................................................. 4 Swedish forestry – the context ................................................................................ 5 SCA forest management and operations ................................................................ 6 Connecting the Red List to SCAs forest management ............................................... 7 About the Swedish Red List 2020 ........................................................................... 7 SCAs species commitment ..................................................................................... 8 Habitat requirements ............................................................................................ 11 Forest management implications .......................................................................... 11 Extent of habitats for redlisted species 2020 ............................................................ 12 Two roundtable discussions ..................................................................................... 13 The road -
Ectomycorrhizal Fungi of Whitebark Pine
14 Ectomycorrhizal fungi of whitebark pine (a tree in peril) revealed by sporocarps and molecular analysis of mycorrhizae from treeline forests in the Greater Yellowstone Ecosystem Katherine R. Mohatt, Cathy L. Cripps, and Matt Lavin Abstract: Whitebark pine (Pinus albicaulis Engelm.) is unique as the only stone pine in North America. This species has declined 40%–90% throughout its range owing to blister rust infection, mountain pine beetle, fire suppression, and global climate change. However, intact mature and old growth forests still exist in the Greater Yellowstone Ecosystem (GYE) at high timberline elevations. This study addresses the urgent need to discover the ectomycorrhizal (ECM) fungi critical to this tree species before forests are further reduced. A study of mature whitebark pine forests across five mountain ranges in the Northern GYE confirmed 32 ECM species of fungi with the pine by sporocarp occurrence in pure stands or by iden- tification of mycorrhizae with ITS-matching. Boletales and Cortinariales (Cortinarius) comprise 50% of the species diver- sity discovered. In Boletales, Suillus subalpinus M.M. Moser (with stone pines), Suillus sibericus Singer (stone pines), Rhizopogon evadens A.H. Sm. (five-needle pines), Rhizopogon spp. (pines) and a semi-secotioid Chroogomphus sp. (pines) are restricted to the hosts listed and are not likely to occur with other high elevation conifers in the GYE. The ascomycete generalist, Cenococcum geophilum Fr., was the most frequent (64%) and abundant (51%) ECM fungus on seedling roots, as previously reported for high elevation spruce-fir and lower elevation lodgepole pine forests in the GYE. The relative importance of the basidiomycete specialists and the ascomycete generalist to whitebark pine (and for seedling establish- ment) is not known, however this study is the first step in delineating the ECM fungi associated with this pine in peril. -
Below-Ground Ectomycorrhizal Community Structure in the Postfire Successional Pinus Koraiensis Forests in the Central Sikhote-Alin (The Russian Far East) Ekaterina F
Botanica Pacifica. A journal of plant science and conservation. 2016. 5(1): 19–31 DOI: 10.17581/bp.2016.05102 Below-ground ectomycorrhizal community structure in the postfire successional Pinus koraiensis forests in the central Sikhote-Alin (the Russian Far East) Ekaterina F. Malysheva 1 *, Vera F. Malysheva 1, Alexander E. Kovalenko 1, Elena A. Pimenova 2, Michael N. Gromyko 3, Svetlana N. Bondarchuk 3 & Elena Yu. Voronina 4 Ekaterina F. Malysheva 1 * ABSTRACT email: [email protected] This study focuses at the effect of forest fire on the extent of ectomycorrhizal Vera F. Malysheva 1 (EcM) colonization of Pinus koraiensis. The EcM fungal diversity was estimated email: [email protected] di rectly from mycorrhizas using molecular techniques. The revealed EcM fun Alexander E. Kovalenko 1 gal community was highly diverse, with 110 operational taxonomic units de tec email: [email protected] ted. The members of Russulaceae and Thelephoraceae were among the most 2 dominant species in both the fire and control sites. The most diverse ba si dio my Elena A. Pimenova cete EcM genera at the burned sites were , , , , email: [email protected] Tomentella Russula Piloderma Inocybe Sui llus, Sebacina and Lactarius. Mycorrhizal colonization was found to be high for Michael N. Gromyko 3 seedlings grown at the burned and the unburned sites. However, there was a ra email: [email protected] ther significant shift between sites in terms of the taxonomic composition of Svetlana N. Bondarchuk 3 EcM symbionts as well as the dominant fungal species. A vertical stratification email: [email protected] of EcM fungal diversity at the control site and the sites of later succession stages 4 was found to be more leveled. -
Phylogenetic and Biogeographic Relationships of Eastern Asian And
Molecular Phylogenetics and Evolution Vol. 17, No. 1, October, pp. 37–47, 2000 doi:10.1006/mpev.2000.0812, available online at http://www.idealibrary.com on Phylogenetic and Biogeographic Relationships of Eastern Asian and Eastern North American Disjunct Suillus Species (Fungi) as Inferred from Nuclear Ribosomal RNA ITS Sequences Qiu-Xin Wu,*,1 Gregory M. Mueller,* Franc¸ois M. Lutzoni,* Yong-Qing Huang,† and Shou-Yu Guo,† *Department of Botany, Field Museum of Natural History, 1400 S. Lake Shore Drive, Chicago, Illinois, 60605-2496; and †Systematic Mycology and Lichenology Laboratory, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100080, People’s Republic of China Received August 24, 1999; revised April 7, 2000 tween putative eastern Asian and eastern North Amer- Species of Suillus produce fleshy, pored mushrooms. ican disjunct species. Wu and Mueller (1997) discussed They are important symbiotic (ectomycorrhizal) part- the north temperate disjunct distributions of some ners of many coniferous trees. The genus includes macrofungi based on morphology and herbarium spec- several putative eastern Asian and eastern North imen records. They concluded that (1) the similarity American disjunct species, i.e., the S. americanus–S. between the mycota of eastern Asia and eastern North sibiricus and S. decipiens–S. spraguei complexes. Phy- America is relatively high as compared to that ob- logenetic relationships among the groups were deter- served between other regions in the north temperate mined to further understand the biogeographic pat- zone; and (2) disjunct distributions of macrofungi are tern. Analyses were based on 40 sequences of the ITS region of the nuclear ribosomal RNA tandem repeats, usually only seen at species or lower taxonomic levels.