XVII SBC LIVRO DE RESUMOS.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

XVII SBC LIVRO DE RESUMOS.Pdf XVII Simpósio de Botânica Criptogâmica XVII SIMPOSIO DE BOTÂNICA CRIPTOGÂMICA LIVRO DE RESUMOS 23>26 SET′09 Tomar [Portugal] 1 XVII Simpósio de Botânica Criptogâmica Jardim Botânico Museu Nacional de História Natural Universidade de Lisboa ISBN: 978-972-96491-8-9 Fotocomposição: J. Cardoso & I. Melo Impressão: RICSIL LDA.—S. João da Talha Capa: TVM - Designers, Lda. 2 23>26 SET′09 Tomar [Portugal] XVII Simpósio de Botânica Criptogâmica COMISSÃO CIENTIFICA COMISSÃO ORGANIZADORA Ana Rosa Burgáz Cecília Sérgio Cecília Sérgio Ireneia Melo Eva Barreno José Cardoso Ignacio Barbara Ana Amorim Ireneia Melo César Garcia Isabel Salcedo Cristina Branquinho Javier Martínez Abaigar Cristina Máguas Leopoldo G. Sancho João Luís Baptista-Ferreira Lília Santos Leena Luís Manuela Sim-Sim Manuela Sim-Sim Margarida Barata Maria Amélia Martins-Loução Maria Teresa Tellería Palmira Carvalho Montserrat Brugués Pedro Pinho Ricardo Melo Rosa Rós Rui Figueira Santiago Fraga Vanda Brotas Vicente Mazimpaka ENTIDADES COLABORADORAS Universidade de Lisboa Jardim Botânico, Museu Nacional de História Natural Departamento de Biologia Vegetal da Faculdade de Ciências Centro de Biologia Ambiental da Faculdade de Ciências Fundação da Universidade de Lisboa Fundação para a Ciência e Tecnologia Fundação Luso-Americana para o Desenvolvimento Câmara Municipal de Tomar 23>26 SET′09 Tomar [Portugal] 3 XVII Simpósio de Botânica Criptogâmica ÍNDICE Programa do Simpósio 6 Resumo das Comunicações: Conferências Plenárias 13 Secção Briologia 21 Secção Ficologia 79 Secção Liquenologia 123 Secção Micologia 177 Secção Pteridologia 213 Disponibilização da Informação 229 Índice dos autores das comunicações 233 Relação dos participantes 239 23>26 SET′09 Tomar [Portugal] XVII Simpósio de Botânica Criptogâmica PROGRAMA—23 SET'09 - QUARTA-FEIRA - SALA DO INFANTE 08:00-09:00 Registo 09:30-10:30 SESSÃO DE ABERTURA 10:30-11:00 Pausa / Café Exploring Cryptogamic Biodiversity under Glo- 11:00-12:00 O. W. PURVIS bal Climate Change / p.15 ECOLOGIA FUNCIONAL E MODELAÇÃO LIQ - P. GIORDANI Numerical approaches to the functional ecology of Mediterranean lichens / p.132 LIQ - - F. GASULLA, A. CALATAYUD, J. REIG- Desiccation tolerance of lichen photobionts is age- ARMIÑANA, F. GARCÍA-BREIJO & E. BARRENO dependent / p.130 12:00-13:00 LIQ - - M. VIVAS , A. PINTADO & L.G. SAN- Differences in photosynthetic performance of popu- CHO lations of Lasallia hispanica (Frey) L.G. Sancho & A. Crespo within an altitudinal gradient from Sierra de Gredos, Central Spain / p.151 FIC - B. MARTÍNEZ, R. VIEJO, S. CALVO & F. Habitat model of Himanthalia elongata: predictions CARREÑO in a warming up scenario / p.95 13:00-14:30 Almoço ECOLOGIA FUNCIONAL E MODELAÇÃO BRI - C. VIEIRA, A. SÉNECA & C. SÉRGIO How functional are bryophyte traits in monitoring stream’s hydrological reality? / p.49 BRI - V. MAZIMPAKA, N. GARCIA MEDINA, R. Tree-age dependent changes among epiphytic LO GIUDICE, R. GARILLETI, I. DRAPER & F. bryophyte communities in Mediterranean environ- LARA ments /p. 40 14:30-15:30 LIQ - - J. RAGGIO, T.G.A. GREEN, A. PINTA- Ecophysiological comparison of different types of DO & L. G. SANCHO crustose lichens adapted to high mountain enviro- ments / p.146 LIQ - - P. PINHO, C. CRUZ, C. MÁGUAS, M.A. Modelling the impact of nitrogen in natural and MARTINS-LOUÇÃO & C. BRANQUINHO semi-natural mediterranean ecosystems using lichens: from local to regional scale / p.142 MONITORIZAÇÃO AMBIENTAL LIQ - - A. B. FERNÁNDEZ-SALEGUI, S.A. Biomonitoreo con Parmelia caperata (L.) Ach. en RODRIGUES, AA. AVELLANOSA SANTOS & A. Asturias (Norte Peninsular) / p.128 TÉRRON ALFONSO LIQ - - S. SAMMUT, I. ÁLVARO, E. LLOP & A. Terricolous Bryophyte and Lichen communities of GÓMEZ-BOLEA two Neolithic Temples in Malta / p.149 15:30-16:30 LIQ - - P. PINHO, C. BRANQUINHO & C. Factors influencing lichen functional-diversity within MÁGUAS a mediterranean forest patch / p.141 MIC - R. TORMO MOLINA, S FERNANDÉZ Yearly and seasonal variation in indoor and outdoor RODRÍGUEZ, A. GONZALO GARRIJO & I. fungus propagules in a hospital / p.186 SILVA PALÁCIOS 16:30-17:00 Pausa / Café 17:00-18:00 POSTERS MICOLOGIA / Sala do Convento WORKSHOP - ALTERAÇÕES CLIMÁTICAS 18:00-19:00 LIQ - - L.G. SANCHO, D. PALÁCIOS, T.G.A. Dating recent deglaciation in Tierra del Fuego using GREEN & A. PINTADO two lichen species with very different growth rates / p.150 19:20-…. Visita à Cidade de Tomar - Porto de honra oferecido pela CMTomar 6 23>26 SET′09 Tomar [Portugal] XVII Simpósio de Botânica Criptogâmica PROGRAMA—23 SET'09 - QUARTA-FEIRA - SALA D. GUALDIM 08:00-09:00 09:30-10:30 10:30-11:00 Pausa / Café 11:00-12:00 SISTEMÁTICA E EVOLUÇÃO BRI - S. RAMS, O. WERNER & R.M. ROS Molecular data support the recognition of the species 'Oreoweisia mulahacenii', an old taxon from Sierra Nevada (Spain) / p.41 BRI - R.M. RÓS, O. WERNER & H. KÖCKIN- Phylogenetical studies in the genus Oxystegus GER (Pottiaceae) / p.42 12:00-1300 BRI - C. LOBO, M. SIM-SIM & M. STECH Molecular studies in Fissidens (Bryophyta) / p.37 BRI - M. SIM-SIM, M. STECH, M.G. ESQUÍ- Molecular, phytochemical and morphological charac- VEL, L. LUÍS, S. FONTINHA, C. LOBO, C. terisation of the liverwort genus Radula in Portugal GARCIA, S. MARTINS, C. VIEIRA, J. BARRO- mainland, Azores and Madeira / p.47 SO, L. PEDRO & A.C.S. FIGUEIREDO 13:00-14:30 Almoço SISTEMÁTICA E EVOLUÇÃO MIC - J. DIÉGUEZ-URIBEONDO & M.P. MAR- Re-evaluación de las especies de Saprolegniales TÍN (Oomicetes) involucradas en la conservación de animales acuáticos amenazados / p.180 FIC - A. GÓMEZ GARRETA, I. BÁRBARA, J. Descripción de las estructuras reproductoras mascu- RULL LLUCH, M.C. BARCELÓ MARTÍ, I. PÉREZ linas de Dictyopteris lucida (Dictyotales, Phaeophy- 14:30-15:30 RUSAFA & M.A. RIBERA SIGUAN ceae) / p.92 FIC - J. CREMADES , I. MANEIRO & R. BAR- Consecuencias de la nueva interpretación taxonómi- REIRO ca del tipo de Plocamium cartilagineum (Plocamiales, Florideophyceae) / p.84 FIC - P. DÍAZ, A. SECILLA, I. BÁRBARA & J. Polysiphonia foetidissima y Polysiphonia sp. en el CREMADES Norte de la costa Atlántica de la Península Ibérica / p.86 SISTEMÁTICA E EVOLUÇÃO FIC - I. FANÉS TREVIÑO, V. SUÁREZ SANTIA- Relaciones entre morfología y filogenia en la familia GO, P.M. SÁNCHEZ CASTILLO & A. COMAS Selenastraceae (Chlorophyceae) / p.88 GONZÁLEZ FIC - M. ABOAL, O. WERNER & J.C. CRISTÓ- Distribución, ecología e identidad taxonómica de BAL Nostoc flagelliforme Berkeley et Curtis in Berkeley / 15:30-16-30 p.81 PTE - A. V. TROITSKY, V.K. BOBROVA, I.A. On marker genes for molecular phylogenetic study of MILYUTINA & S. YU MOROZOV Selaginellaceae / p.218 PTE - A. JIMÉNEZ, R. HOLDEREGGER, D. Microsatellites reveal extreme inbreeding in the CSENCSICS & L.G. QUINTANILLA diploid fern Dryopteris aemula / p.216 16:30-17:00 Pausa / Café 23>26 SET′09 Tomar [Portugal] 7 XVII Simpósio de Botânica Criptogâmica PROGRAMA—24 SET'09 - QUINTA-FEIRA - SALA DO INFANTE MONITORIZAÇÃO AMBIENTAL FIC - A. REY-ASENSIO, I. G. VIANA, C. CAR- δ15N en macroalgas como marcador del área de BALLEIRA & A. CARBALLEIRA influencia de los vertidos de piscifactorías marinas instaladas en tierra / p.97 FIC - I. GONZÁLEZ VIANA, J.R. ABOAL, J. A. Utilización de las macroalgas del Banco de Especi- FERNÁNDEZ, C. REAL, R. VILLARES & A. CAR- menes Ambientales de Galicia (BEAG) en la aplica- BALLEIRA ción de la Directiva Marco del Agua / p.93 FIC - N. FLOR-ARNAU, GALÁN-CUBERO, P. Evolución del estado ecológico del agua en el río ORTIZ-LERÍN, J. CAMBRA-SÁNCHEZ & C. Ebro en el período 2007-2008 utilizando las Diato- DURAN LALAGUNA meas como bioindicadores / p.89 09:00-10:30 FIC - M.R. DE ORTE, C. CARBALLEIRA & A. Desarrollo de un bioensayo miniaturizado de CARBALLEIRA microalgas para evaluar la ecotoxicidad de vertidos marinos: Aplicación a piscifactorías marinas instala- das en tierra / p.85 FIC - P. SÁNCHEZ CASTILLO, F. BULLEJOS, S. Comunidades epilíticas en lagos de alta montaña ROSILLO, I. SEGUÍ, E. MERLONI, E. LINARES, como biomonitores del cambio global / p.99 N. KORBEE, F.L. FIGUEROA, M. VILLAR, J.M. MEDINA SÁNCHEZ & P. CARRILLO FIC - J. CAMBRA-SÁNCHEZ, A. GALÁN- Evaluación de la calidad ecológica del agua en el río CUBERO, N. FLOR-ARNAU, R. ORTIZ-LERÍN, E. Ebro utilizando los macrófitos como bioindicadores / VELASCO-BATLLE & C. DURAN-LALAGUNA p.82 10:30-11:00 Pausa / Café CONFERÊNCIA PLENÁRIA S. ROBBERT GRADSTEIN Influence of deforestation and global warming 11:00-12:00 on tropical bryophytes / p.16 MONITORIZAÇÃO AMBIENTAL BRI - J. Á. FERNÁNDEZ, J.R. ABOAL & A. CAR- Biomonitorización de la contaminación atmosférica BALLEIRA con musgos terrestres: necesidad de una armoniza- ción metodológica / p.29 BRI - J. MARTÍNEZ-ABAIGAR, R. TOMÁS, G. Utilización de la hepática acuática Jungermannia FABÓN & E. NÚÑEZ-OLIVERA exsertifolia subsp. cordifolia como bioindicador de 12:00-13:00 radiación ultravioleta / p.39 BRI - R. CRUZ DE CARVALHO, M. CATALÃ, E. Desiccation physiology of Fontinalis antipyretica: BARRENO, C. BRANQUINHO & J. MARQUES DA Oxidative stress / p.27 SILVA BRI - J.R. ABOAL, M.T. BOQUETE, J.A. FER- ¿Permiten estimar los musgos terrestres la deposi- NÁNDEZ & A. CARBALLEIRA ción atmosférica de metales pesados? / p.23 13:00-14:30 Almoço CONFERÊNCIA PLENÁRIA 14:30-15:30 D. J. PATTERSON Future Taxonomy / p.17 BIODIVERSIDADE E CONSERVAÇÃO BRI - S. CALVO ARANDA, R. GABRIEL, J.M. The bryophyte flora of the Azorean Archipelago: How LOBO & P.A.V. BORGES much stays for discovering? / p.26 BRI - A. BERGAMINI The 2010 biodiversity target and the Swiss bryophy- te flora: Assessment of trends / p.24 BRI - C. GARCIA, C. SÉRGIO, M. SIM-SIM & F. Flora Briológica do Arquipélago de São Tomé e Prín- LARA 15:30-16:30 cipe. Primeira caracterização das comunidades brio- fíticas / p.31 BRI - L. LUÍS, M. SIM-SIM, R. FIGUEIRA & A. Contribution to the conservation and management of BERGAMINI water resources in mountainous islands from Maca- ronesian: The case of stream bryophyte communi- ties from Madeira Island / p.38 16:30-17:00 Pausa / Café 17:00-18:00 POSTERS FICOLOGIA E PTERIDOLOGIA / Sala do Convento WORKSHOP - DISPONIBILAZAÇÃO DA INFORMAÇÃO 18:00-19:00 F.
Recommended publications
  • Phylogeny of the Cetrarioid Core (Parmeliaceae) Based on Five
    The Lichenologist 41(5): 489–511 (2009) © 2009 British Lichen Society doi:10.1017/S0024282909990090 Printed in the United Kingdom Phylogeny of the cetrarioid core (Parmeliaceae) based on five genetic markers Arne THELL, Filip HÖGNABBA, John A. ELIX, Tassilo FEUERER, Ingvar KÄRNEFELT, Leena MYLLYS, Tiina RANDLANE, Andres SAAG, Soili STENROOS, Teuvo AHTI and Mark R. D. SEAWARD Abstract: Fourteen genera belong to a monophyletic core of cetrarioid lichens, Ahtiana, Allocetraria, Arctocetraria, Cetraria, Cetrariella, Cetreliopsis, Flavocetraria, Kaernefeltia, Masonhalea, Nephromopsis, Tuckermanella, Tuckermannopsis, Usnocetraria and Vulpicida. A total of 71 samples representing 65 species (of 90 worldwide) and all type species of the genera are included in phylogentic analyses based on a complete ITS matrix and incomplete sets of group I intron, -tubulin, GAPDH and mtSSU sequences. Eleven of the species included in the study are analysed phylogenetically for the first time, and of the 178 sequences, 67 are newly constructed. Two phylogenetic trees, one based solely on the complete ITS-matrix and a second based on total information, are similar, but not entirely identical. About half of the species are gathered in a strongly supported clade composed of the genera Allocetraria, Cetraria s. str., Cetrariella and Vulpicida. Arctocetraria, Cetreliopsis, Kaernefeltia and Tuckermanella are monophyletic genera, whereas Cetraria, Flavocetraria and Tuckermannopsis are polyphyletic. The taxonomy in current use is compared with the phylogenetic results, and future, probable or potential adjustments to the phylogeny are discussed. The single non-DNA character with a strong correlation to phylogeny based on DNA-sequences is conidial shape. The secondary chemistry of the poorly known species Cetraria annae is analyzed for the first time; the cortex contains usnic acid and atranorin, whereas isonephrosterinic, nephrosterinic, lichesterinic, protolichesterinic and squamatic acids occur in the medulla.
    [Show full text]
  • Checklist of Calicioid Lichens and Fungi for Genera with Members in Temperate Western North America Draft: 2012-03-13
    Draft: 2012-03-13 Checklist of Calicioids – E. B. Peterson Checklist of Calicioid Lichens and Fungi For Genera with Members in Temperate Western North America Draft: 2012-03-13 by E. B. Peterson Calicium abietinum, EBP#4640 1 Draft: 2012-03-13 Checklist of Calicioids – E. B. Peterson Genera Acroscyphus Lév. Brucea Rikkinen Calicium Pers. Chaenotheca Th. Fr. Chaenothecopsis Vainio Coniocybe Ach. = Chaenotheca "Cryptocalicium" – potentially undescribed genus; taxonomic placement is not known but there are resemblances both to Mycocaliciales and Onygenales Cybebe Tibell = Chaenotheca Cyphelium Ach. Microcalicium Vainio Mycocalicium Vainio Phaeocalicium A.F.W. Schmidt Sclerophora Chevall. Sphinctrina Fr. Stenocybe (Nyl.) Körber Texosporium Nádv. ex Tibell & Hofsten Thelomma A. Massal. Tholurna Norman Additional genera are primarily tropical, such as Pyrgillus, Tylophoron About the Species lists Names in bold are believed to be currently valid names. Old synonyms are indented and listed with the current name following (additional synonyms can be found in Esslinger (2011). Names in quotes are nicknames for undescribed species. Names given within tildes (~) are published, but may not be validly published. Underlined species are included in the checklist for North America north of Mexico (Esslinger 2011). Names are given with authorities and original citation date where possible, followed by a colon. Additional citations are given after the colon, followed by a series of abbreviations for states and regions where known. States and provinces use the standard two-letter abbreviation. Regions include: NAm = North America; WNA = western North America (west of the continental divide); Klam = Klamath Region (my home territory). For those not known from North America, continental distribution may be given: SAm = South America; EUR = Europe; ASIA = Asia; Afr = Africa; Aus = Australia.
    [Show full text]
  • (63) Continuation Inspart of Application No. PCT RE"SE SEN"I", "ES"E"NE
    US 2010.0086647A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2010/0086647 A1 Kristiansen (43) Pub. Date: Apr. 8, 2010 (54) FEED OR FOOD PRODUCTS COMPRISING filed on Jan. 25, 2006, provisional application No. FUNGALMATERAL 60/690,496, filed on Jun. 15, 2005. (75) Inventor: Bjorn Kristiansen, Frederikstad (30) Foreign Application Priority Data (NO) May 13, 2005 (DK) ........................... PA 2005 00710 Correspondence Address: Jun. 15, 2005 (DK). ... PA 2005 OO88O BROWDY AND NEIMARK, P.L.L.C. Jul. 15, 2005 (DK) ....................... PCTFDKO5/OO498 624 NINTH STREET, NW Jan. 25, 2006 (DK)........................... PA 2006 OO117 SUTE 300 WASHINGTON, DC 20001-5303 (US) Publication Classification 51) Int. Cl. (73)73) AssigneeA : MEDMUSHAS(DK) s HORSHOLM ( A2.3L I/28 (2006.01) A23K L/18 (2006.01) (21) Appl. No.: 11/914,318 A23K L/6 (2006.01) CI2P 19/04 (2006.01) (22) PCT Filed: May 11, 2006 AOIK 6L/00 (2006.01) (86). PCT NO. PCT/DKO6/OO2S3 (52) U.S. Cl. ................................ 426/62: 426/2: 119/230 S371 (c)(1) (57) ABSTRACT (2), (4) Date: Dec. 1, 2009 The present invention relates to feed and food compositions comprising material obtained by fermenting fungi of the Related U.S. Application Data Basidiomycetes family in a liquid medium. Interestingly, (63) DK2005/000498,continuation inspart filed onof Jul.application 15, 2005. No. PCT enhanceRE"SE Survival SEN"I",and/or support "ES"E"NE growth of normal, healthy (60) Provisional application No. 60/690,496, filed on Jun. animals. Furthermore, the compounds may modulate the 15, 2005, provisional application No.
    [Show full text]
  • Aleurodiscus Bicornis and A. Formosanus Spp. Nov. (Basidiomycota) with Smooth Basidiospores, and Description of A
    Aleurodiscus Bicornis and A. Formosanus Spp. Nov. (Basidiomycota) With Smooth Basidiospores, and Description of A. Parvisporus From NE China Sheng-Hua Wu ( [email protected] ) National Museum of Natural Science https://orcid.org/0000-0002-9873-5595 Chia-Ling Wei National Museum of Natural Science, ROC Chiung-Chih Chang Biodiversity Research Institute Research Article Keywords: China, corticioid fungi, Taiwan, taxonomy, wood-decaying fungi Posted Date: March 22nd, 2021 DOI: https://doi.org/10.21203/rs.3.rs-306327/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/18 Abstract Three species of Aleurodiscus s.l. characterized in having effused basidiomata, clamped generative hyphae and quasi-binding hyphae, sulphuric positive reaction of gloeocystidia, hyphidia, acanthophyses and smooth basidiospores, are described. They are A. bicornis sp. nov., A. formosanus sp. nov. and A. parvisporus. Aleurodiscus bicornis was found from high mountains of NW Yunnan Province of SW China, grew on branch of Picea sp. Aleurodiscus formosanus was found from high mountains of central Taiwan, grew on branch of gymnosperm. Aleurodiscus parvisporus was previously reported only once from Japan and Sichuan Province of China respectively, and is reported in this study from Jilin Province of China. Phylogenetic relationships of these three species were inferred from analyses of a combined dataset consisting of three genetic markers, viz. 28S, nuc rDNA ITS1-5.8S-ITS2 (ITS), and a portion of the translation elongation factor 1-alpha gene, TEF1. The studied three species are phylogenetically closely related with signicant support, corresponds with resemblance of their morphological features.
    [Show full text]
  • (2014), Volume 2, Issue 11, 238-245
    ISSN 2320-5407 International Journal of Advanced Research (2014), Volume 2, Issue 11, 238-245 Journal homepage: http://www.journalijar.com INTERNATIONAL JOURNAL OF ADVANCED RESEARCH RESEARCH ARTICLE Diversity of family Meruliaceae from Jammu Division (J&K), India Jyoti*, Avneet Pal Singh & Gurpaul Singh Dhingra Department of Botany, Punjabi University, Patiala, 147002 India Manuscript Info Abstract Manuscript History: An account of eight resupinate, non-poroid taxa (Crustoderma corneum, Gyrophanopsis polonensis, Hyphoderma argillaceum, H. hjortstamii, H. Received: 25 September 2014 Final Accepted: 19 October 2014 setigerum, H. setigerum var. bicystidium, Hypochnicium wakefieldiae, Published Online: November 2014 Radulodon indicus) of family Meruliaceae (Class- Agaricomycetes, Phylum- Basidiomycota) has been given. All these are new reports for the Key words: Jammu Division in the state of Jammu and Kashmir (J&K). Of these, Basidiomycota, Agaricomycetes, Hyphoderma hjortstamii is a new record for India, Hypochnicium Meruliaceae. wakefieldiae new for the North Western Himalaya, Crustoderma corneum, Gyrophanopsis polonensis and H. setigerum var. bicystidium new for J&K. *Corresponding Author Jyoti Sharma Copy Right, IJAR, 2014,. All rights reserved Introduction While conducting fungal forays in the different localities of Jammu division in the state of Jammu and Kashmir (India), twelve collections of resupinate, non-poroid Agaricomycetous fungi were made. On the basis of comparison of macroscopic and microscopic features in the published literature (Thind & Rattan 1970, Eriksson & Ryvarden 1975, Rattan 1977, Eriksson & Ryvarden 1976, Eriksson et al. 1981, Wu SH. 1990, Stalpers 1998, Nakasone 2001, Bernicchia & Gorjón 2010), these have been identified as Crustoderma corneum, Gyrophanopsis polonensis, Hyphoderma argillaceum, H. hjortstamii, H. setigerum, H. setigerum var. bicystidium, Hypochnicium wakefieldiae and Radulodon indicus.
    [Show full text]
  • Basidiomycota) in Finland
    Mycosphere 7 (3): 333–357(2016) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/7/3/7 Copyright © Guizhou Academy of Agricultural Sciences Extensions of known geographic distribution of aphyllophoroid fungi (Basidiomycota) in Finland Kunttu P1, Kulju M2, Kekki T3, Pennanen J4, Savola K5, Helo T6 and Kotiranta H7 1University of Eastern Finland, School of Forest Sciences, P.O. Box 111, FI-80101 Joensuu, Finland 2Biodiversity Unit P.O. Box 3000, FI-90014 University of Oulu, Finland 3Jyväskylä University Museum, Natural History Section, P.O. BOX 35, FI-40014 University of Jyväskylä, Finland 4Pentbyntie 1 A 2, FI-10300 Karjaa, Finland 5The Finnish Association for Nature Conservation, Itälahdenkatu 22 b A, FI-00210 Helsinki, Finland 6Erätie 13 C 19, FI-87200 Kajaani, Finland 7Finnish Environment Institute, P.O. Box 140, FI-00251 Helsinki, Finland Kunttu P, Kulju M, Kekki T, Pennanen J, Savola K, Helo T, Kotiranta H 2016 – Extensions of known geographic distribution of aphyllophoroid fungi (Basidiomycota) in Finland. Mycosphere 7(3), 333–357, Doi 10.5943/mycosphere/7/3/7 Abstract This article contributes the knowledge of Finnish aphyllophoroid funga with nationally or regionally new species, and records of rare species. Ceriporia bresadolae, Clavaria tenuipes and Renatobasidium notabile are presented as new aphyllophoroid species to Finland. Ceriporia bresadolae and R. notabile are globally rare species. The records of Ceriporia aurantiocarnescens, Crustomyces subabruptus, Sistotrema autumnale, Trechispora elongata, and Trechispora silvae- ryae are the second in Finland. New records (or localities) are provided for 33 species with no more than 10 records in Finland. In addition, 76 records of aphyllophoroid species are reported as new to some subzones of the boreal vegetation zone in Finland.
    [Show full text]
  • Species Relationships and Farina Evolution in the Cheilanthoid Fern
    Systematic Botany (2011), 36(3): pp. 554–564 © Copyright 2011 by the American Society of Plant Taxonomists DOI 10.1600/036364411X583547 Species Relationships and Farina Evolution in the Cheilanthoid Fern Genus Argyrochosma (Pteridaceae) Erin M. Sigel , 1 , 3 Michael D. Windham , 1 Layne Huiet , 1 George Yatskievych , 2 and Kathleen M. Pryer 1 1 Department of Biology, Duke University, Durham, North Carolina 27708 U. S. A. 2 Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri 63166 U. S. A. 3 Author for correspondence ( [email protected] ) Communicating Editor: Lynn Bohs Abstract— Convergent evolution driven by adaptation to arid habitats has made it difficult to identify monophyletic taxa in the cheilanthoid ferns. Dependence on distinctive, but potentially homoplastic characters, to define major clades has resulted in a taxonomic conundrum: all of the largest cheilanthoid genera have been shown to be polyphyletic. Here we reconstruct the first comprehensive phylogeny of the strictly New World cheilanthoid genus Argyrochosma . We use our reconstruction to examine the evolution of farina (powdery leaf deposits), which has played a prominent role in the circumscription of cheilanthoid genera. Our data indicate that Argyrochosma comprises two major monophyletic groups: one exclusively non-farinose and the other primarily farinose. Within the latter group, there has been at least one evolutionary reversal (loss) of farina and the development of major chemical variants that characterize specific clades. Our phylogenetic hypothesis, in combination with spore data and chromosome counts, also provides a critical context for addressing the prevalence of polyploidy and apomixis within the genus. Evidence from these datasets provides testable hypotheses regarding reticulate evolution and suggests the presence of several previ- ously undetected taxa of Argyrochosma.
    [Show full text]
  • 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.
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2009/0005340 A1 Kristiansen (43) Pub
    US 20090005340A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2009/0005340 A1 Kristiansen (43) Pub. Date: Jan. 1, 2009 54) BOACTIVE AGENTS PRODUCED BY 3O Foreigngn AppApplication PrioritVty Data SUBMERGED CULTIVATION OFA BASDOMYCETE CELL Jun. 15, 2005 (DK) ........................... PA 2005 OO881 Jan. 25, 2006 (DK)........................... PA 2006 OO115 (75) Inventor: Bjorn Kristiansen, Frederikstad Publication Classification (NO)NO (51) Int. Cl. Correspondence Address: A 6LX 3L/75 (2006.01) BROWDY AND NEIMARK, P.L.L.C. CI2P I/02 (2006.01) 624 NINTH STREET, NW A6IP37/00 (2006.01) SUTE 300 CI2P 19/04 (2006.01) WASHINGTON, DC 20001-5303 (US) (52) U.S. Cl. ............................ 514/54:435/171; 435/101 (57) ABSTRACT (73) Assignee: MediMush A/S, Horsholm (DK) - The invention in one aspect is directed to a method for culti (21) Appl. No.: 11/917,516 Vating a Basidiomycete cell in liquid culture medium, said method comprising the steps of providing a Basidiomycete (22) PCT Filed: Jun. 14, 2006 cell capable of being cultivated in a liquid growth medium, e - rs and cultivating the Basidiomycete cell under conditions (86). PCT No.: PCT/DK2OO6/OOO340 resulting in the production intracellularly or extracellularly of one or more bioactive agent(s) selected from the group con S371 (c)(1) sisting of oligosaccharides, polysaccharides, optionally gly (2), (4) Date: Ul. 31, 2008 cosylated peptides or polypeptides, oligonucleotides, poly s e a v-9 nucleotides, lipids, fatty acids, fatty acid esters, secondary O O metabolites Such as polyketides, terpenes, steroids, shikimic Related U.S. Application Data acids, alkaloids and benzodiazepine, wherein said bioactive (60) Provisional application No.
    [Show full text]
  • Lichens and Associated Fungi from Glacier Bay National Park, Alaska
    The Lichenologist (2020), 52,61–181 doi:10.1017/S0024282920000079 Standard Paper Lichens and associated fungi from Glacier Bay National Park, Alaska Toby Spribille1,2,3 , Alan M. Fryday4 , Sergio Pérez-Ortega5 , Måns Svensson6, Tor Tønsberg7, Stefan Ekman6 , Håkon Holien8,9, Philipp Resl10 , Kevin Schneider11, Edith Stabentheiner2, Holger Thüs12,13 , Jan Vondrák14,15 and Lewis Sharman16 1Department of Biological Sciences, CW405, University of Alberta, Edmonton, Alberta T6G 2R3, Canada; 2Department of Plant Sciences, Institute of Biology, University of Graz, NAWI Graz, Holteigasse 6, 8010 Graz, Austria; 3Division of Biological Sciences, University of Montana, 32 Campus Drive, Missoula, Montana 59812, USA; 4Herbarium, Department of Plant Biology, Michigan State University, East Lansing, Michigan 48824, USA; 5Real Jardín Botánico (CSIC), Departamento de Micología, Calle Claudio Moyano 1, E-28014 Madrid, Spain; 6Museum of Evolution, Uppsala University, Norbyvägen 16, SE-75236 Uppsala, Sweden; 7Department of Natural History, University Museum of Bergen Allégt. 41, P.O. Box 7800, N-5020 Bergen, Norway; 8Faculty of Bioscience and Aquaculture, Nord University, Box 2501, NO-7729 Steinkjer, Norway; 9NTNU University Museum, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway; 10Faculty of Biology, Department I, Systematic Botany and Mycology, University of Munich (LMU), Menzinger Straße 67, 80638 München, Germany; 11Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK; 12Botany Department, State Museum of Natural History Stuttgart, Rosenstein 1, 70191 Stuttgart, Germany; 13Natural History Museum, Cromwell Road, London SW7 5BD, UK; 14Institute of Botany of the Czech Academy of Sciences, Zámek 1, 252 43 Průhonice, Czech Republic; 15Department of Botany, Faculty of Science, University of South Bohemia, Branišovská 1760, CZ-370 05 České Budějovice, Czech Republic and 16Glacier Bay National Park & Preserve, P.O.
    [Show full text]
  • Phylogeny, Taxonomy and Diversification Events in the Caliciaceae
    Fungal Diversity DOI 10.1007/s13225-016-0372-y Phylogeny, taxonomy and diversification events in the Caliciaceae Maria Prieto1,2 & Mats Wedin1 Received: 21 December 2015 /Accepted: 19 July 2016 # The Author(s) 2016. This article is published with open access at Springerlink.com Abstract Although the high degree of non-monophyly and Calicium pinicola, Calicium trachyliodes, Pseudothelomma parallel evolution has long been acknowledged within the occidentale, Pseudothelomma ocellatum and Thelomma mazaediate Caliciaceae (Lecanoromycetes, Ascomycota), a brunneum. A key for the mazaedium-producing Caliciaceae is natural re-classification of the group has not yet been accom- included. plished. Here we constructed a multigene phylogeny of the Caliciaceae-Physciaceae clade in order to resolve the detailed Keywords Allocalicium gen. nov. Calicium fossil . relationships within the group, to propose a revised classification, Divergence time estimates . Lichens . Multigene . and to perform a dating study. The few characters present in the Pseudothelomma gen. nov available fossil and the complex character evolution of the group affects the interpretation of morphological traits and thus influ- ences the assignment of the fossil to specific nodes in the phy- Introduction logeny, when divergence time analyses are carried out. Alternative fossil assignments resulted in very different time es- Caliciaceae is one of several ascomycete groups characterized timates and the comparison with the analysis based on a second- by producing prototunicate (thin-walled and evanescent) asci ary calibration demonstrates that the most likely placement of the and a mazaedium (an accumulation of loose, maturing spores fossil is close to a terminal node rather than a basal placement in covering the ascoma surface).
    [Show full text]
  • 9B Taxonomy to Genus
    Fungus and Lichen Genera in the NEMF Database Taxonomic hierarchy: phyllum > class (-etes) > order (-ales) > family (-ceae) > genus. Total number of genera in the database: 526 Anamorphic fungi (see p. 4), which are disseminated by propagules not formed from cells where meiosis has occurred, are presently not grouped by class, order, etc. Most propagules can be referred to as "conidia," but some are derived from unspecialized vegetative mycelium. A significant number are correlated with fungal states that produce spores derived from cells where meiosis has, or is assumed to have, occurred. These are, where known, members of the ascomycetes or basidiomycetes. However, in many cases, they are still undescribed, unrecognized or poorly known. (Explanation paraphrased from "Dictionary of the Fungi, 9th Edition.") Principal authority for this taxonomy is the Dictionary of the Fungi and its online database, www.indexfungorum.org. For lichens, see Lecanoromycetes on p. 3. Basidiomycota Aegerita Poria Macrolepiota Grandinia Poronidulus Melanophyllum Agaricomycetes Hyphoderma Postia Amanitaceae Cantharellales Meripilaceae Pycnoporellus Amanita Cantharellaceae Abortiporus Skeletocutis Bolbitiaceae Cantharellus Antrodia Trichaptum Agrocybe Craterellus Grifola Tyromyces Bolbitius Clavulinaceae Meripilus Sistotremataceae Conocybe Clavulina Physisporinus Trechispora Hebeloma Hydnaceae Meruliaceae Sparassidaceae Panaeolina Hydnum Climacodon Sparassis Clavariaceae Polyporales Gloeoporus Steccherinaceae Clavaria Albatrellaceae Hyphodermopsis Antrodiella
    [Show full text]