Evolutionary Trends in Basidiomycota

Total Page:16

File Type:pdf, Size:1020Kb

Evolutionary Trends in Basidiomycota ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Stapfia Jahr/Year: 2012 Band/Volume: 0096 Autor(en)/Author(s): Oberwinkler Franz Artikel/Article: Evolutionary trends in Basidiomycota 45-104 ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Evolutionary trends in Basidiomycota FRANZ OBERWINKLER* Abstract ! " aP!% !"&' ! "" ( )" " )\" )"!""+ !!N -! " '" .!" "aPaP %"" " "\N /! " )!!2"'""/" -!" 3") aP&" +N-"" 6 Zusammenfassung2)89) !!%.!) !2)=!"%! '!!>!"%" !") a2)P"!)82)" &)"!> 2)8!") >)82)"363" ?>93 '!)>)' !/']))8 STAPFIA 96 (2012) | 45 ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 )!'!"=+2! 8!" )'!I)" )""(")8 "!(!)JN 82)=)' )"(!" "2])"! .".6)8)?)" aPaP)( %6?=3) !!2)3)%%6)) )=!)!>N=% !%=%9 >!"2)K%]) -!8%)=])" 9!(!)"(!) ?"69K)/6(!) L3!69"8 2)"/E 2])%"=I %!(!)]!)J ')!(N"K)) "%>)8 !!'" N-!!6) ! Key words""" *&)!M6 /!"I"(G"NOPNQ"K INTRODUCTION ! a9(6 !6 2)" (6 -36 6 ) P" !66!] a! 3 /!6 P ] ]" - " !" Phytophthora % 6 6 " 6 ! + 6 " " \ E" ! ]" 6 a P DE BARY (1884) " " 6 ( a()P F'GH 46 | STAPFIA 96 (2012) ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 1\! FHF!H "&'"" )!]"()F(H )'"/"3!" =&F. OBERWINKLER. OG" PN GVPP6GNPP(6 Arabidopsis thali- Phytophthora infestans 6 anaKURAMAEFOPPQH HAMPLFOPPUH" )"+6 \ 6! 6 &' N a 6!" 6 6 & ' F' OH /6! \PCAV- 6 6 ALIER-SMITH FOPGPH" \ 6 + FLUTZONIOPPR"JAMES N- PARFREY OPPQ" HIBBETT OPPN" STAJICH !"BALDAUF FOPGGH OPPU" WANG OPPUH 3" FOPPSH \ " 6 (6 " I! 6 +" /! ) FT L! + ()H".=6F.6 )] 6 )" " =H ! ! FLEFÈVRE OPPNH" /"a GOPP() &FJONES STAPFIA 96 (2012) | RN ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 2&'6 !UPP6GOPP(FH- ]. &'!LIUFOPPQH" ]K !"6 &F. OBERWINKLER OPGGH"6 SO 2"Coprinopsis F Copri- LN " nus) cinereus Laccaria bicolor FITZPATRICK "WANG FOPPQHWRV"SOU FOPPUH"GPPX6 + + RO6 " L a 6 \ 6 "6 ) + " J6 6 6 " =6 - " Puc- !P 2)) cinia graminis Sporobolomyces (CUOMO & BIRREN OPGPH N = roseus 26 GPPX ' 6 " Ustilago maydis Malassezia Coprinopsis cinereus, Sac- Ustilago maydis, Crypto- globosa I" Cryp- charomyces cerevisiae Schizosac- coccus neoformans, Phanerochaete tocococcus neoformans C. gattii charomyces pombe, BURNSFOPGPH chrysosporium, Coprinopsis F Co- " Phanerochaete chrys- prinus) cinereus 6 osporium Postia placenta VPPNUPP 48 | STAPFIA 96 (2012) ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 3&\&'/!)!&6 &]=J6 K3" FDEN BAKKEROPGPH6 )/"Geosiphon pyriforme"!Nostoc6 " / 6)6 FLUTZONIOPPGH )) )" /F. OBERWINKLER & 6 6 Evolutionary trends: ! 3"RPP( . &" Pa- !6 leopyrenomycites devonicus (TAYLOR KY TAYLOR & BERBEE FOPPQH OPPVH" ]Z] VP =" %Z OV" LÜCKING /ZZ FOPPUH Y6 6 6 Paleopyrenomycites6 ] NQP 6 68Y( 6 (GPQ"&"J6 &6 OPP( K 6 +"6 Y QPP6NPP(" + RPP(" VPP6QVP( STAPFIA 96 (2012) | RU ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 4!"a'!86 RPP3Asteroxylon !6FHb- !d-L !eL6 "caTAYLOR FGUUUH/F. OBERWINKLER Dikarya " (KNIEP GUOSH ) 6 6 8!+ Armillaria gallica ! F' WH HODNETT & ANDERSON FOPPPH I 6 ! 3" " ] -6 ! ! 6 !"6 ! ! ANDERSON & KOHN (2007) " ! " 6 6 ! !" " -"6 6 !6 - 50 | STAPFIA 96 (2012) ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 5: Microbotryum saponariae" FH/F. OBERWINKLER "!6 ! " ! " )!6 FOH FOBER- FBULLERGUWP"GUWGH" FWH WINKLER GUNSH N FQUINTANILHA 1937, FR"VH"6 RAPER 1966)-" FQHL 6 6 6 " 6 FANDERSON & KOHN 2007). 6 WG"PPP - F'R"V"H" (KIRKOPPSH36 " L +)! F GÄUMANN FPRIN- GUQRH GLEOPPVH= YANGFOPGGH " F' R H aL P" Basidiomycota Sporobolomy- Evolution of morphological ces (KLUYVER & VAN NIELGUOR"GUONH" structures 6 Sporidiobolus (NYLANDGURUH" ) 6 = F'R""H N - ! " " ! + " !" FGH" \ 6 STAPFIA 96 (2012) | 51 ©Biologiezentrum Linz, Austria, download www.biologiezentrum.at OBERWINKLER# STAPFIA 96 (2012): 45–104 Fig. 6: Conocybe subovata (aHC. lactea (b6fHab=6 +FHc2 d8 e>)f!66 FH\OP3GP3/F.
Recommended publications
  • Mycoparasitism Between Squamanita Paradoxa and Cystoderma Amianthinum (Cystodermateae, Agaricales)
    Mycoscience (2010) 51:456–461 DOI 10.1007/s10267-010-0052-9 SHORT COMMUNICATION Mycoparasitism between Squamanita paradoxa and Cystoderma amianthinum (Cystodermateae, Agaricales) P. Brandon Matheny • Gareth W. Griffith Received: 1 January 2010 / Accepted: 23 March 2010 / Published online: 13 April 2010 Ó The Mycological Society of Japan and Springer 2010 Abstract Circumstantial evidence, mostly morphological from basidiocarps or parasitized galls or tissue of other and ecological, points to ten different mushroom host agarics. On occasion, chimeric fruitbodies appear obvious, species for up to fifteen species of the mycoparasitic genus as in S. paradoxa (A.H. Sm. & Singer) Bas (Fig. 1), but for Squamanita. Here, molecular evidence confirms Cysto- other species, the hosts are unknown (Table 1). It appears derma amianthinum as the host for S. paradoxa, a spo- that in all cases, galls induced by Squamanita mycelium radically occurring and rarely collected mycoparasite with contain chlamydospores, and the term protocarpic tuber has extreme host specificity. This is only the second study to been replaced by the term cecidiocarp (Bas and Thoen use molecular techniques to reveal or confirm the identity 1998). Hosts of Squamanita include distantly related of a cecidiocarp of Squamanita species. Phylogenetic species of Agaricales, such as Galerina Earle, Inocybe (Fr.) analysis of combined nuclear ribosomal RNA genes sug- Fr., Hebeloma (Fr.) P. Kumm., Kuehneromyces Singer & gests the monophyly of Squamanita, Cystoderma, and A.H. Sm., and Amanita Pers. However, Squamanita also Phaeolepiota, a clade referred to as the tribe Cystoder- parasitizes species of Phaeolepiota Maire ex Konrad & mateae. If true, S. paradoxa and C. amianthinum would Maubl.
    [Show full text]
  • Two New Chrysomyxa Rust Species on the Endemic Plant, Picea Asperata in Western China, and Expanded Description of C
    Phytotaxa 292 (3): 218–230 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.292.3.2 Two new Chrysomyxa rust species on the endemic plant, Picea asperata in western China, and expanded description of C. succinea JING CAO1, CHENG-MING TIAN1, YING-MEI LIANG2 & CHONG-JUAN YOU1* 1The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University, Beijing 100083, China 2Museum of Beijing Forestry University, Beijing 100083, China *Corresponding author: [email protected] Abstract Two new rust species, Chrysomyxa diebuensis and C. zhuoniensis, on Picea asperata are recognized by morphological characters and DNA sequence data. A detailed description, illustrations, and discussion concerning morphologically similar and phylogenetically closely related species are provided for each species. From light and scanning electron microscopy observations C. diebuensis is characterized by the nailhead to peltate aeciospores, with separated stilt-like base. C. zhuoni- ensis differs from other known Chrysomyxa species in the annulate aeciospores with distinct longitudinal smooth cap at ends of spores, as well as with a broken, fissured edge. Analysis based on internal transcribed spacer region (ITS) partial gene sequences reveals that the two species cluster as a highly supported group in the phylogenetic trees. Correlations between the morphological and phylogenetic features are discussed. Illustrations and a detailed description are also provided for the aecia of C. succinea in China for the first time. Keywords: aeciospores, molecular phylogeny, spruce needle rust, taxonomy Introduction Picea asperata Mast.is native to western China, widely distributed in Qinghai, Gansu, Shaanxi and western Sichuan.
    [Show full text]
  • Clarification of the Life-Cycle of Chrysomyxa Woroninii on Ledum
    Mycol. Res. 104 (5): 581–586 (May 2000). Printed in the United Kingdom. 581 Clarification of the life-cycle of Chrysomyxa woroninii on Ledum and Picea Patricia E. CRANE1, 2, Yasuyuki HIRATSUKA2 and Randolph S. CURRAH1 " Department of Biological Sciences, University of Alberta, Edmonton, AB T6G 2E9, Canada # Northern Forestry Centre, Canadian Forest Service, 5320-122 Street, Edmonton, AB T6H 3S5, Canada. Accepted 5 August 1999. The rust fungus Chrysomyxa woroninii causes perennial witches’ brooms on several species of Ledum in northern and subalpine regions of Europe, North America and Asia. Spruce bud rust has been assumed to be the aecial state of C. woroninii because of the close proximity of infected Ledum plants and systemically infected buds on Picea. The lack of experimental evidence for this connection, however, and the presence of other species of Chrysomyxa on the same hosts has led to confusion about the life-cycle of C. woroninii. In this study, infections on both spruce and Ledum were studied in the field and in a greenhouse. The link between the two states was proven by inoculating spruce with basidiospores from Ledum groenlandicum. After infection of spruce in spring, probably through the needles, the fungus overwinters in the unopened buds until the next spring, when the infected shoots are distinguished by stunting and yellow or red discolouration. Microscopic examination of dormant Ledum shoots showed that C. woroninii overwinters in this host in the bracts and outer leaves of the vegetative buds, and in the pith and cortex of the stem. The telia of C. woroninii, on systemically infected Ledum leaves of the current season, are easily distinguished from the telia of other Chrysomyxa species on the same hosts.
    [Show full text]
  • Revision of the Genus Cotylidia (Basidiomycota, Hymenochaetales) in the Czech Republic
    CZECH MYCOLOGY 65(1): 1–13, JUNE 10, 2013 (ONLINE VERSION, ISSN 1805-1421) Revision of the genus Cotylidia (Basidiomycota, Hymenochaetales) in the Czech Republic 1 2 JIŘÍ KOUT *, LUCIE ZÍBAROVÁ 1Department of Biology, Geosciences and Environmental Education, Faculty of Education, University of West Bohemia, Klatovská 51, Plzeň, CZ-306 19, Czech Republic; [email protected] 2Department of Botany, Faculty of Natural Sciences, University of South Bohemia, Na Zlaté stoce 1, České Budějovice, CZ-370 05, Czech Republic; [email protected] *corresponding author Kout J., Zíbarová L. (2013): Revision of the genus Cotylidia (Basidiomycota, Hymenochaetales) in the Czech Republic. – Czech Mycol. 65(1): 1–13. To date, three species of the genus Cotylidia have been identified in the Czech Republic: C. muscigena, C. pannosa, and C. undulata. The occurrence of Cotylidia undulata in the Czech Re- public was already confirmed and a new locality is published here. The other two species are newly re- ported from the Czech Republic. The remaining two European Cotylidia species are not yet known from the area studied: C. carpatica and the badly known Mediterranean C. marsicana. Finally one specimen found during the study of herbarium material does not correspond well to any known Euro- pean species. The genus was reviewed based on fresh and herbarium specimens. The species of Cotylidia are described and an identification key is added. All three species are rarely reported fungi. Key words: hymenochaetoid clade, taxonomy, distribution, threatened fungi, Europe. Kout J., Zíbarová L. (2013): Revize rodu lupénka – Cotylidia (Basidiomycota, Hymenochaetales) v České republice. – Czech Mycol. 65(1): 1–13.
    [Show full text]
  • Appendix K. Survey and Manage Species Persistence Evaluation
    Appendix K. Survey and Manage Species Persistence Evaluation Establishment of the 95-foot wide construction corridor and TEWAs would likely remove individuals of H. caeruleus and modify microclimate conditions around individuals that are not removed. The removal of forests and host trees and disturbance to soil could negatively affect H. caeruleus in adjacent areas by removing its habitat, disturbing the roots of host trees, and affecting its mycorrhizal association with the trees, potentially affecting site persistence. Restored portions of the corridor and TEWAs would be dominated by early seral vegetation for approximately 30 years, which would result in long-term changes to habitat conditions. A 30-foot wide portion of the corridor would be maintained in low-growing vegetation for pipeline maintenance and would not provide habitat for the species during the life of the project. Hygrophorus caeruleus is not likely to persist at one of the sites in the project area because of the extent of impacts and the proximity of the recorded observation to the corridor. Hygrophorus caeruleus is likely to persist at the remaining three sites in the project area (MP 168.8 and MP 172.4 (north), and MP 172.5-172.7) because the majority of observations within the sites are more than 90 feet from the corridor, where direct effects are not anticipated and indirect effects are unlikely. The site at MP 168.8 is in a forested area on an east-facing slope, and a paved road occurs through the southeast part of the site. Four out of five observations are more than 90 feet southwest of the corridor and are not likely to be directly or indirectly affected by the PCGP Project based on the distance from the corridor, extent of forests surrounding the observations, and proximity to an existing open corridor (the road), indicating the species is likely resilient to edge- related effects at the site.
    [Show full text]
  • Cystoderma Amianthinum Cystoderma
    © Demetrio Merino Alcántara [email protected] Condiciones de uso Cystoderma amianthinum (Scop.) Fayod, Annls Sci. Nat., Bot., sér. 7 9: 351 (1889) Agaricaceae, Agaricales, Agaricomycetidae, Agaricomycetes, Agaricomycotina, Basidiomycota, Fungi ≡ Agaricus amianthinus Scop., Fl. carniol., Edn 2 (Wien) 2: 434 (1772) ≡ Agaricus amianthinus Scop., Fl. carniol., Edn 2 (Wien) 2: 434 (1772) var. amianthinus ≡ Agaricus amianthinus var. broadwoodiae Berk. & Broome, Ann. Mag. nat. Hist., Ser. 5 3: 202 (1879) ≡ Agaricus granulosus var. amianthinus (Scop.) Fr., Epicr. syst. mycol. (Upsaliae): 18 (1838) [1836-1838] = Agaricus rugosoreticulatum F. Lorinser, Öst. bot. Z. 29: 23 (1879) ≡ Armillaria amianthina (Scop.) Kauffman, Pap. Mich. Acad. Sci. 2: 60 (1923) [1922] = Armillaria rugosoreticulata (F. Lorinser) Zeller [as 'rugoso-reticulata'], Mycologia 25(5): 378 (1933) ≡ Cystoderma amianthinum (Scop.) Konrad & Maubl., Icon. Select. Fung. 6(3): pl. 238 (1927) ≡ Cystoderma amianthinum f. album (Maire) A.H. Sm. & Singer, Pap. Mich. Acad. Sci. 30: 112 (1945) [1944] ≡ Cystoderma amianthinum (Scop.) Fayod, Annls Sci. Nat., Bot., sér. 7 9: 351 (1889) f. amianthinum ≡ Cystoderma amianthinum f. olivaceum Singer, Pap. Mich. Acad. Sci. 30: 111 (1945) [1944] ≡ Cystoderma amianthinum f. rugosoreticulatum (F. Lorinser) A.H. Sm. & Singer, Pap. Mich. Acad. Sci. 30: 110 (1945) [1944] ≡ Cystoderma amianthinum f. rugosoreticulatum (F. Lorinser) Bon [as 'rugulosoreticulatum'], Bull. trimest. Soc. mycol. Fr. 86(1): 99 (1970) ≡ Cystoderma amianthinum (Scop.) Fayod, Annls Sci. Nat., Bot., sér. 7 9: 351 (1889) var. amianthinum ≡ Cystoderma amianthinum var. rugosoreticulatum (F. Lorinser) Bon, Docums Mycol. 29(no. 115): 34 (1999) = Cystoderma longisporum f. rugosoreticulatum (F. Lorinser) Heinem. & Thoen [as 'rugoso-reticulatum'], Bull. trimest. Soc. mycol. Fr. 89(1): 31 (1973) = Cystoderma rugosoreticulatum (F.
    [Show full text]
  • How Many Fungi Make Sclerotia?
    fungal ecology xxx (2014) 1e10 available at www.sciencedirect.com ScienceDirect journal homepage: www.elsevier.com/locate/funeco Short Communication How many fungi make sclerotia? Matthew E. SMITHa,*, Terry W. HENKELb, Jeffrey A. ROLLINSa aUniversity of Florida, Department of Plant Pathology, Gainesville, FL 32611-0680, USA bHumboldt State University of Florida, Department of Biological Sciences, Arcata, CA 95521, USA article info abstract Article history: Most fungi produce some type of durable microscopic structure such as a spore that is Received 25 April 2014 important for dispersal and/or survival under adverse conditions, but many species also Revision received 23 July 2014 produce dense aggregations of tissue called sclerotia. These structures help fungi to survive Accepted 28 July 2014 challenging conditions such as freezing, desiccation, microbial attack, or the absence of a Available online - host. During studies of hypogeous fungi we encountered morphologically distinct sclerotia Corresponding editor: in nature that were not linked with a known fungus. These observations suggested that Dr. Jean Lodge many unrelated fungi with diverse trophic modes may form sclerotia, but that these structures have been overlooked. To identify the phylogenetic affiliations and trophic Keywords: modes of sclerotium-forming fungi, we conducted a literature review and sequenced DNA Chemical defense from fresh sclerotium collections. We found that sclerotium-forming fungi are ecologically Ectomycorrhizal diverse and phylogenetically dispersed among 85 genera in 20 orders of Dikarya, suggesting Plant pathogens that the ability to form sclerotia probably evolved 14 different times in fungi. Saprotrophic ª 2014 Elsevier Ltd and The British Mycological Society. All rights reserved. Sclerotium Fungi are among the most diverse lineages of eukaryotes with features such as a hyphal thallus, non-flagellated cells, and an estimated 5.1 million species (Blackwell, 2011).
    [Show full text]
  • The Diversity of Basidiomycota Fungi That Have the Potential As a Source of Nutraceutical to Be Developed in the Concept of Integrated Forest Management Poisons
    International Journal of Recent Technology and Engineering (IJRTE) ISSN: 2277-3878, Volume-8 Issue-2S, July 2019 The Diversity of Basidiomycota Fungi that Have the Potential as a Source of Nutraceutical to be Developed in the Concept of Integrated Forest Management Mustika Dewi, I Nyoman Pugeg Aryantha, Mamat Kandar straw mushrooms, oyster mushrooms, and shiitake Abstract: The fungus Basidiomycota found in Indonesia have mushrooms. very high diversity, but have not been explored so far. The development of local Basidiomycota mushrooms that Development of fungi Basidiomycota is an alternative as a are cultivated by utilizing space on the forest floor has not source of natural nutraceuticals, especially beta glucan and been done mostly in Indonesia. In several countries such as lovastatin compounds. This compound can be used in the pharmaceutical and food fields. This study aims to obtain Japan, people have long been cultivating shitake mushrooms Basidiomycota fungi isolates that have the potential as a by utilizing forest floors. Reported by (Savoie & Largeteau, nutraceutical source. As the first stage in this research, the 2011) that mushrooms from the Basidiomycota group are activities carried out were exploration, isolation on culture widely produced in forest areas through the utilization of media, and identification of fungi based on genotypic forest floors as a place to grow these fungi which have characters. The results showed that the fungi identified based on economic value quite high by applying the concept of their genotypic characters were Pleurotusostreatus, Ganodermacf, Resinaceum, Lentinulaedodes, micosilviculture. The concept of micosilviculture is a Vanderbyliafraxinea, Auricularia delicate, Pleurotusgiganteus, concept that is applied in the management of integrated Auricularia sp.
    [Show full text]
  • The Flora Mycologica Iberica Project Fungi Occurrence Dataset
    A peer-reviewed open-access journal MycoKeys 15: 59–72 (2016)The Flora Mycologica Iberica Project fungi occurrence dataset 59 doi: 10.3897/mycokeys.15.9765 DATA PAPER MycoKeys http://mycokeys.pensoft.net Launched to accelerate biodiversity research The Flora Mycologica Iberica Project fungi occurrence dataset Francisco Pando1, Margarita Dueñas1, Carlos Lado1, María Teresa Telleria1 1 Real Jardín Botánico-CSIC, Claudio Moyano 1, 28014, Madrid, Spain Corresponding author: Francisco Pando ([email protected]) Academic editor: C. Gueidan | Received 5 July 2016 | Accepted 25 August 2016 | Published 13 September 2016 Citation: Pando F, Dueñas M, Lado C, Telleria MT (2016) The Flora Mycologica Iberica Project fungi occurrence dataset. MycoKeys 15: 59–72. doi: 10.3897/mycokeys.15.9765 Resource citation: Pando F, Dueñas M, Lado C, Telleria MT (2016) Flora Mycologica Iberica Project fungi occurrence dataset. v1.18. Real Jardín Botánico (CSIC). Dataset/Occurrence. http://www.gbif.es/ipt/resource?r=floramicologicaiberi ca&v=1.18, http://doi.org/10.15468/sssx1e Abstract The dataset contains detailed distribution information on several fungal groups. The information has been revised, and in many times compiled, by expert mycologist(s) working on the monographs for the Flora Mycologica Iberica Project (FMI). Records comprise both collection and observational data, obtained from a variety of sources including field work, herbaria, and the literature. The dataset contains 59,235 records, of which 21,393 are georeferenced. These correspond to 2,445 species, grouped in 18 classes. The geographical scope of the dataset is Iberian Peninsula (Continental Portugal and Spain, and Andorra) and Balearic Islands. The complete dataset is available in Darwin Core Archive format via the Global Biodi- versity Information Facility (GBIF).
    [Show full text]
  • Fruiting Body Form, Not Nutritional Mode, Is the Major Driver of Diversification in Mushroom-Forming Fungi
    Fruiting body form, not nutritional mode, is the major driver of diversification in mushroom-forming fungi Marisol Sánchez-Garcíaa,b, Martin Rybergc, Faheema Kalsoom Khanc, Torda Vargad, László G. Nagyd, and David S. Hibbetta,1 aBiology Department, Clark University, Worcester, MA 01610; bUppsala Biocentre, Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, SE-75005 Uppsala, Sweden; cDepartment of Organismal Biology, Evolutionary Biology Centre, Uppsala University, 752 36 Uppsala, Sweden; and dSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, 6726 Szeged, Hungary Edited by David M. Hillis, The University of Texas at Austin, Austin, TX, and approved October 16, 2020 (received for review December 22, 2019) With ∼36,000 described species, Agaricomycetes are among the and the evolution of enclosed spore-bearing structures. It has most successful groups of Fungi. Agaricomycetes display great di- been hypothesized that the loss of ballistospory is irreversible versity in fruiting body forms and nutritional modes. Most have because it involves a complex suite of anatomical features gen- pileate-stipitate fruiting bodies (with a cap and stalk), but the erating a “surface tension catapult” (8, 11). The effect of gas- group also contains crust-like resupinate fungi, polypores, coral teroid fruiting body forms on diversification rates has been fungi, and gasteroid forms (e.g., puffballs and stinkhorns). Some assessed in Sclerodermatineae, Boletales, Phallomycetidae, and Agaricomycetes enter into ectomycorrhizal symbioses with plants, Lycoperdaceae, where it was found that lineages with this type of while others are decayers (saprotrophs) or pathogens. We constructed morphology have diversified at higher rates than nongasteroid a megaphylogeny of 8,400 species and used it to test the following lineages (12).
    [Show full text]
  • Phylum Order Number of Species Number of Orders Family Genus Species Japanese Name Properties Phytopathogenicity Date Pref
    Phylum Order Number of species Number of orders family genus species Japanese name properties phytopathogenicity date Pref. points R inhibition H inhibition R SD H SD Basidiomycota Polyporales 98 12 Meruliaceae Abortiporus Abortiporus biennis ニクウチワタケ saprobic "+" 2004-07-18 Kumamoto Haru, Kikuchi 40.4 -1.6 7.6 3.2 Basidiomycota Agaricales 171 1 Meruliaceae Abortiporus Abortiporus biennis ニクウチワタケ saprobic "+" 2004-07-16 Hokkaido Shari, Shari 74 39.3 2.8 4.3 Basidiomycota Agaricales 269 1 Agaricaceae Agaricus Agaricus arvensis シロオオハラタケ saprobic "-" 2000-09-25 Gunma Kawaba, Tone 87 49.1 2.4 2.3 Basidiomycota Polyporales 181 12 Agaricaceae Agaricus Agaricus bisporus ツクリタケ saprobic "-" 2004-04-16 Gunma Horosawa, Kiryu 36.2 -23 3.6 1.4 Basidiomycota Hymenochaetales 129 8 Agaricaceae Agaricus Agaricus moelleri ナカグロモリノカサ saprobic "-" 2003-07-15 Gunma Hirai, Kiryu 64.4 44.4 9.6 4.4 Basidiomycota Polyporales 105 12 Agaricaceae Agaricus Agaricus moelleri ナカグロモリノカサ saprobic "-" 2003-06-26 Nagano Minamiminowa, Kamiina 70.1 3.7 2.5 5.3 Basidiomycota Auriculariales 37 2 Agaricaceae Agaricus Agaricus subrutilescens ザラエノハラタケ saprobic "-" 2001-08-20 Fukushima Showa 67.9 37.8 0.6 0.6 Basidiomycota Boletales 251 3 Agaricaceae Agaricus Agaricus subrutilescens ザラエノハラタケ saprobic "-" 2000-09-25 Yamanashi Hakusyu, Hokuto 80.7 48.3 3.7 7.4 Basidiomycota Agaricales 9 1 Agaricaceae Agaricus Agaricus subrutilescens ザラエノハラタケ saprobic "-" 85.9 68.1 1.9 3.1 Basidiomycota Hymenochaetales 129 8 Strophariaceae Agrocybe Agrocybe cylindracea ヤナギマツタケ saprobic "-" 2003-08-23
    [Show full text]
  • Aquatic and Wet Marchantiophyta, Order Metzgeriales: Aneuraceae
    Glime, J. M. 2021. Aquatic and Wet Marchantiophyta, Order Metzgeriales: Aneuraceae. Chapt. 1-11. In: Glime, J. M. Bryophyte 1-11-1 Ecology. Volume 4. Habitat and Role. Ebook sponsored by Michigan Technological University and the International Association of Bryologists. Last updated 11 April 2021 and available at <http://digitalcommons.mtu.edu/bryophyte-ecology/>. CHAPTER 1-11: AQUATIC AND WET MARCHANTIOPHYTA, ORDER METZGERIALES: ANEURACEAE TABLE OF CONTENTS SUBCLASS METZGERIIDAE ........................................................................................................................................... 1-11-2 Order Metzgeriales............................................................................................................................................................... 1-11-2 Aneuraceae ................................................................................................................................................................... 1-11-2 Aneura .......................................................................................................................................................................... 1-11-2 Aneura maxima ............................................................................................................................................................ 1-11-2 Aneura mirabilis .......................................................................................................................................................... 1-11-7 Aneura pinguis ..........................................................................................................................................................
    [Show full text]