Guttova&Al Layout 1
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Study on Rare and Noteworthy Lichenized Ascomycetes from Sardinia (Italy)
©Biologiezentrum Linz, Austria; download unter www.zobodat.at NEUWIRTH • Noteworthy lichenized ascomycetes from Sardinia STAPFIA 109 (2018): 181–196 A study on rare and noteworthy lichenized ascomycetes from Sardinia (Italy) GERHARD NEUWIRTH* Abstract: The study reports about remarkable lichen species from the Mediterranean region, collected from various substrates during a one-week trip through Sardinia in May 2018. One of them was recorded for the first time in Sardinia and thirty-two lichenized ascomycetes could be classified as either extremely rare, very rare or rare. The aim of this publication is to contribute to the lichen flora by means of a photographic documentation including short comments on rare species and additional information about the collecting sites. A species list of all recorded taxa is provided. Zusammenfassung: Die Studie berichtet über bemerkenswerte Flechtenarten aus dem Mittelmeerraum, gesammelt auf verschiedenen Substraten während einer einwöchigen Fahrt durch Sardinien im Mai 2018. Eine Art wurde erstmals in Sardinien belegt und 32 lichenisierte Ascomyceten konnten als extrem selten bis selten eingeordnet werden. Das Ziel dieser Publikation ist ein Beitrag zur Flechtenflora mithilfe einer fotografischen Dokumentation inklusive kurzer Kommentare über seltene Arten und zusätzliche Informationen über den Fundort. Eine Liste aller belegten Taxa wird zur Verfügung gestellt. Key words: Mediterranean region, rare records, taxonomy, photographic documentation. 1Correspondence to: [email protected] Rabenberg 18, 4911 Tumeltsham, Austria INTRODUCTION Modern literature on these topics refers to ZEDDA & SIPMAN (2001) who discussed a special group of lichens on Juniperus The second largest island of the Mediterranean region cove- oxycedrus. NIMIS & MARTELLOS (2002) provided a key for the 2 res an area of 24,090 km and is characterized by a high diversity identification of terricolous lichens in Italy. -
New Records of Crustose Teloschistaceae (Lichens, Ascomycota) from the Murmansk Region of Russia
vol. 37, no. 3, pp. 421–434, 2016 doi: 10.1515/popore-2016-0022 New records of crustose Teloschistaceae (lichens, Ascomycota) from the Murmansk region of Russia Ivan FROLOV1* and Liudmila KONOREVA2,3 1 Department of Botany, Faculty of Science, University of South Bohemia, Branišovská 31, České Budějovice, CZ-37005, Czech Republic 2 Laboratory of Flora and Vegetations, The Polar-Alpine Botanical Garden and Institute KSC RAS, Kirovsk, Murmansk region, 184209, Russia 3 Laboratory of Lichenology and Bryology, Komarov Botanical Institute RAS, Professor Popov St. 2, St. Petersburg, 197376, Russia * corresponding author <[email protected]> Abstract: Twenty-three species of crustose Teloschistaceae were collected from the northwest of the Murmansk region of Russia during field trips in 2013 and 2015. Blas- tenia scabrosa is a new combination supported by molecular data. Blastenia scabrosa, Caloplaca fuscorufa and Flavoplaca havaasii are new to Russia. Blastenia scabrosa is also new to the Caucasus Mts and Sweden. Detailed morphological measurements of the Russian specimens of these species are provided. Caloplaca exsecuta, C. grimmiae and C. sorocarpa are new to the Murmansk region. The taxonomic position of C. alcarum is briefly discussed. Key words: Arctic, Rybachy Peninsula, Caloplaca s. lat., Blastenia scabrosa. Introduction Although the Murmansk region is one of the best studied regions of Russia in terms of lichen diversity, there are numerous reports in recent literature of new discoveries there (e.g. Fadeeva et al. 2013; Konoreva 2015; Melechin 2015; Urbanavichus 2015). Several localities in the northwest of the Murmansk region, mainly on the Pechenga Tundra Mountains and the Rybachy Peninsula, were visited in 2013 and 2015. -
1307 Fungi Representing 1139 Infrageneric Taxa, 317 Genera and 66 Families ⇑ Jolanta Miadlikowska A, , Frank Kauff B,1, Filip Högnabba C, Jeffrey C
Molecular Phylogenetics and Evolution 79 (2014) 132–168 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families ⇑ Jolanta Miadlikowska a, , Frank Kauff b,1, Filip Högnabba c, Jeffrey C. Oliver d,2, Katalin Molnár a,3, Emily Fraker a,4, Ester Gaya a,5, Josef Hafellner e, Valérie Hofstetter a,6, Cécile Gueidan a,7, Mónica A.G. Otálora a,8, Brendan Hodkinson a,9, Martin Kukwa f, Robert Lücking g, Curtis Björk h, Harrie J.M. Sipman i, Ana Rosa Burgaz j, Arne Thell k, Alfredo Passo l, Leena Myllys c, Trevor Goward h, Samantha Fernández-Brime m, Geir Hestmark n, James Lendemer o, H. Thorsten Lumbsch g, Michaela Schmull p, Conrad L. Schoch q, Emmanuël Sérusiaux r, David R. Maddison s, A. Elizabeth Arnold t, François Lutzoni a,10, Soili Stenroos c,10 a Department of Biology, Duke University, Durham, NC 27708-0338, USA b FB Biologie, Molecular Phylogenetics, 13/276, TU Kaiserslautern, Postfach 3049, 67653 Kaiserslautern, Germany c Botanical Museum, Finnish Museum of Natural History, FI-00014 University of Helsinki, Finland d Department of Ecology and Evolutionary Biology, Yale University, 358 ESC, 21 Sachem Street, New Haven, CT 06511, USA e Institut für Botanik, Karl-Franzens-Universität, Holteigasse 6, A-8010 Graz, Austria f Department of Plant Taxonomy and Nature Conservation, University of Gdan´sk, ul. Wita Stwosza 59, 80-308 Gdan´sk, Poland g Science and Education, The Field Museum, 1400 S. -
An Evolving Phylogenetically Based Taxonomy of Lichens and Allied Fungi
Opuscula Philolichenum, 11: 4-10. 2012. *pdf available online 3January2012 via (http://sweetgum.nybg.org/philolichenum/) An evolving phylogenetically based taxonomy of lichens and allied fungi 1 BRENDAN P. HODKINSON ABSTRACT. – A taxonomic scheme for lichens and allied fungi that synthesizes scientific knowledge from a variety of sources is presented. The system put forth here is intended both (1) to provide a skeletal outline of the lichens and allied fungi that can be used as a provisional filing and databasing scheme by lichen herbarium/data managers and (2) to announce the online presence of an official taxonomy that will define the scope of the newly formed International Committee for the Nomenclature of Lichens and Allied Fungi (ICNLAF). The online version of the taxonomy presented here will continue to evolve along with our understanding of the organisms. Additionally, the subfamily Fissurinoideae Rivas Plata, Lücking and Lumbsch is elevated to the rank of family as Fissurinaceae. KEYWORDS. – higher-level taxonomy, lichen-forming fungi, lichenized fungi, phylogeny INTRODUCTION Traditionally, lichen herbaria have been arranged alphabetically, a scheme that stands in stark contrast to the phylogenetic scheme used by nearly all vascular plant herbaria. The justification typically given for this practice is that lichen taxonomy is too unstable to establish a reasonable system of classification. However, recent leaps forward in our understanding of the higher-level classification of fungi, driven primarily by the NSF-funded Assembling the Fungal Tree of Life (AFToL) project (Lutzoni et al. 2004), have caused the taxonomy of lichen-forming and allied fungi to increase significantly in stability. This is especially true within the class Lecanoromycetes, the main group of lichen-forming fungi (Miadlikowska et al. -
Lichen Functional Trait Variation Along an East-West Climatic Gradient in Oregon and Among Habitats in Katmai National Park, Alaska
AN ABSTRACT OF THE THESIS OF Kaleigh Spickerman for the degree of Master of Science in Botany and Plant Pathology presented on June 11, 2015 Title: Lichen Functional Trait Variation Along an East-West Climatic Gradient in Oregon and Among Habitats in Katmai National Park, Alaska Abstract approved: ______________________________________________________ Bruce McCune Functional traits of vascular plants have been an important component of ecological studies for a number of years; however, in more recent times vascular plant ecologists have begun to formalize a set of key traits and universal system of trait measurement. Many recent studies hypothesize global generality of trait patterns, which would allow for comparison among ecosystems and biomes and provide a foundation for general rules and theories, the so-called “Holy Grail” of ecology. However, the majority of these studies focus on functional trait patterns of vascular plants, with a minority examining the patterns of cryptograms such as lichens. Lichens are an important component of many ecosystems due to their contributions to biodiversity and their key ecosystem services, such as contributions to mineral and hydrological cycles and ecosystem food webs. Lichens are also of special interest because of their reliance on atmospheric deposition for nutrients and water, which makes them particularly sensitive to air pollution. Therefore, they are often used as bioindicators of air pollution, climate change, and general ecosystem health. This thesis examines the functional trait patterns of lichens in two contrasting regions with fundamentally different kinds of data. To better understand the patterns of lichen functional traits, we examined reproductive, morphological, and chemical trait variation along precipitation and temperature gradients in Oregon. -
Steciana Doi:10.12657/Steciana.020.008 ISSN 1689-653X
2016, Vol. 20(2): 63–72 Steciana doi:10.12657/steciana.020.008 www.up.poznan.pl/steciana ISSN 1689-653X LICHENS AS INDICATORS OF AIR POLLUTION IN ŁOMŻA ANNA MATWIEJUK, PAULINA CHOJNOWSKA A. Matwiejuk, P. Chojnowska, Institute of Biology, University of Bialystok, Konstanty Ciołkowski 1 J, 15-245 Białystok, Poland, e-mail: [email protected], [email protected] (Received: December 9, 2015. Accepted: March 29, 2016) ABSTRACT. Research using lichens as bioindicators of air pollution has been conducted in the city of Łomża. The presence of indicator species of epiphytic and epilithic lichens has been analysed. A 4-point lichen scale has been developed for the test area, on the basis of which four lichenoindication zones have been deter- mined. The least favourable conditions for lichen growth have been recorded in the city center. Green areas and open spaces are the areas with the most favourable impact of the urban environment on lichen biota. KEY WORDS: air pollution, biodiversity, lichens, urban environment INTRODUCTION terised by high resistance to factors such as extreme temperatures, lack of water and short growing peri- Lichens (lichenized fungi, Fungi lichenisati) are symbi- od, yet highest sensitivity to air pollution (Fałtyno otic organisms, created in most cases by an associa- wicz 1995). For more than 140 years lichens have tion of green algae (Chlorophyta) or blue-green algae been considered one of the best bioindicators of air (Cyanobacteria) and fungi, especially ascomycetes pollution (NYLANDER 1866). (Ascomycota) (NASH 1996, PURVIS 2000). They are Areas with particularly heavy impact of civili- mushrooms with a specific nutritional strategy, in- zation on the environment are cities. -
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. -
Huneckia Pollinii </I> and <I> Flavoplaca Oasis
MYCOTAXON ISSN (print) 0093-4666 (online) 2154-8889 Mycotaxon, Ltd. ©2017 October–December 2017—Volume 132, pp. 895–901 https://doi.org/10.5248/132.895 Huneckia pollinii and Flavoplaca oasis newly recorded from China Cong-Cong Miao 1#, Xiang-Xiang Zhao1#, Zun-Tian Zhao1, Hurnisa Shahidin2 & Lu-Lu Zhang1* 1 Key Laboratory of Plant Stress Research, College of Life Sciences, Shandong Normal University, Jinan, 250014, P. R. China 2 Lichens Research Center in Arid Zones of Northwestern China, College of Life Science and Technology, Xinjiang University, Xinjiang , 830046 , P. R. China * Correspondence to: [email protected] Abstract—Huneckia pollinii and Flavoplaca oasis are described and illustrated from Chinese specimens. The two species and the genus Huneckia are recorded for the first time from China. Keywords—Asia, lichens, taxonomy, Teloschistaceae Introduction Teloschistaceae Zahlbr. is one of the larger families of lichenized fungi. It includes three subfamilies, Caloplacoideae, Teloschistoideae, and Xanthorioideae (Gaya et al. 2012; Arup et al. 2013). Many new genera have been proposed based on molecular phylogenetic investigations (Arup et al. 2013; Fedorenko et al. 2012; Gaya et al. 2012; Kondratyuk et al. 2013, 2014a,b, 2015a,b,c,d). Currently, the family contains approximately 79 genera (Kärnefelt 1989; Arup et al. 2013; Kondratyuk et al. 2013, 2014a,b, 2015a,b,c,d; Søchting et al. 2014a,b). Huneckia S.Y. Kondr. et al. was described in 2014 (Kondratyuk et al. 2014a) based on morphological, anatomical, chemical, and molecular data. It is characterized by continuous to areolate thalli, paraplectenchymatous cortical # Cong-Cong Miao & Xiang-Xiang Zhao contributed equally to this research. -
Catenarina (Teloschistaceae, Ascomycota), a New Southern Hemisphere Genus with 7-Chlorocatenarin
The Lichenologist 46(2): 175–187 (2014) 6 British Lichen Society, 2014 doi:10.1017/S002428291300087X Catenarina (Teloschistaceae, Ascomycota), a new Southern Hemisphere genus with 7-chlorocatenarin Ulrik SØCHTING, Majbrit Zeuthen SØGAARD, John A. ELIX, Ulf ARUP, Arve ELVEBAKK and Leopoldo G. SANCHO Abstract: A new genus, Catenarina (Teloschistaceae, Ascomycota), with three species is described from the Southern Hemisphere, supported by molecular data. All species contain the secondary metabolite 7-chlorocatenarin, previously unknown in lichens. Catenarina desolata is a non-littoral, lichenicolous species found on volcanic and soft sedimentary rock at 190–300 m in and near steppes in southernmost Chile and on the subantarctic island, Kerguelen. Catenarina vivasiana grows on maritime rocks and on rock outcrops in lowland Nothofagus forests, but has also been found at alti- tudes up to c. 580 m on moss and detritus on outcrops in Tierra del Fuego. The Antarctic species Caloplaca iomma is transferred to Catenarina based on chemical data; it grows on rocks near the coast in maritime Antarctica. Key words: Antarctica, Argentina, Caloplaca, Chile, HPLC, Kerguelen Island, lichen metabolites, molecular phylogeny Accepted for publication 18 November 2013 Introduction circumscribe with classical morphological, anatomical and secondary chemical char- The lichen family Teloschistaceae, with more acters. However, in some cases, secondary than 1000 species published worldwide metabolites provide synapomorphic charac- (Søchting & Lutzoni 2003; Gaya et al. ters, such as in the genus Shackletonia (Arup 2012), is currently receiving considerable et al. 2013). attention in order to subdivide the family Tierra del Fuego and southern Patagonia into molecularly-based genera (Arup et al. have recently been subjected to intensive 2013). -
<I> Lecanoromycetes</I> of Lichenicolous Fungi Associated With
Persoonia 39, 2017: 91–117 ISSN (Online) 1878-9080 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE https://doi.org/10.3767/persoonia.2017.39.05 Phylogenetic placement within Lecanoromycetes of lichenicolous fungi associated with Cladonia and some other genera R. Pino-Bodas1,2, M.P. Zhurbenko3, S. Stenroos1 Key words Abstract Though most of the lichenicolous fungi belong to the Ascomycetes, their phylogenetic placement based on molecular data is lacking for numerous species. In this study the phylogenetic placement of 19 species of cladoniicolous species lichenicolous fungi was determined using four loci (LSU rDNA, SSU rDNA, ITS rDNA and mtSSU). The phylogenetic Pilocarpaceae analyses revealed that the studied lichenicolous fungi are widespread across the phylogeny of Lecanoromycetes. Protothelenellaceae One species is placed in Acarosporales, Sarcogyne sphaerospora; five species in Dactylosporaceae, Dactylo Scutula cladoniicola spora ahtii, D. deminuta, D. glaucoides, D. parasitica and Dactylospora sp.; four species belong to Lecanorales, Stictidaceae Lichenosticta alcicorniaria, Epicladonia simplex, E. stenospora and Scutula epiblastematica. The genus Epicladonia Stictis cladoniae is polyphyletic and the type E. sandstedei belongs to Leotiomycetes. Phaeopyxis punctum and Bachmanniomyces uncialicola form a well supported clade in the Ostropomycetidae. Epigloea soleiformis is related to Arthrorhaphis and Anzina. Four species are placed in Ostropales, Corticifraga peltigerae, Cryptodiscus epicladonia, C. galaninae and C. cladoniicola -
A Multigene Phylogenetic Synthesis for the Class Lecanoromycetes (Ascomycota): 1307 Fungi Representing 1139 Infrageneric Taxa, 317 Genera and 66 Families
A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families Miadlikowska, J., Kauff, F., Högnabba, F., Oliver, J. C., Molnár, K., Fraker, E., ... & Stenroos, S. (2014). A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families. Molecular Phylogenetics and Evolution, 79, 132-168. doi:10.1016/j.ympev.2014.04.003 10.1016/j.ympev.2014.04.003 Elsevier Version of Record http://cdss.library.oregonstate.edu/sa-termsofuse Molecular Phylogenetics and Evolution 79 (2014) 132–168 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A multigene phylogenetic synthesis for the class Lecanoromycetes (Ascomycota): 1307 fungi representing 1139 infrageneric taxa, 317 genera and 66 families ⇑ Jolanta Miadlikowska a, , Frank Kauff b,1, Filip Högnabba c, Jeffrey C. Oliver d,2, Katalin Molnár a,3, Emily Fraker a,4, Ester Gaya a,5, Josef Hafellner e, Valérie Hofstetter a,6, Cécile Gueidan a,7, Mónica A.G. Otálora a,8, Brendan Hodkinson a,9, Martin Kukwa f, Robert Lücking g, Curtis Björk h, Harrie J.M. Sipman i, Ana Rosa Burgaz j, Arne Thell k, Alfredo Passo l, Leena Myllys c, Trevor Goward h, Samantha Fernández-Brime m, Geir Hestmark n, James Lendemer o, H. Thorsten Lumbsch g, Michaela Schmull p, Conrad L. Schoch q, Emmanuël Sérusiaux r, David R. Maddison s, A. Elizabeth Arnold t, François Lutzoni a,10, -
A Provisional Checklist of the Lichens of Belarus
Opuscula Philolichenum, 17: 374-479. 2018. *pdf effectively published online 31December2018 via (http://sweetgum.nybg.org/philolichenum/) A Provisional Checklist of the Lichens of Belarus ANDREI TSURYKAU1 ABSTRACT. – A total of 606 species and five subspecific taxa of lichens and allied fungi are documented from Belarus based on combined historical (pre-1980) and modern (post-1980) records. Of these, 50 (8.3%) are represented by only historical reports, 235 (38.8%) are represented by only modern vouchers, and 310 (51.2%) are represented by both historical and modern records. Eleven species are known only from generalized published reports that lacked specific location data. Eighty-eight species are excluded as erroneous reports, or considered as doubtful records. KEYWORDS. – Biodiversity, distribution, lichenized fungi, historical baseline. INTRODUCTION Published accounts of the lichens of Belarus date to the end of the 18th century (Gilibert 1781). In the first phase of lichenological discovery in the country (1780–1900) lichens did not attract special attention and were reported among the general lists of vascular plants and fungi. However, 49 species were reported by the French botanist J.E. Gilibert, the Russian ethnographer of Belarusian origin N. Downar (Dovnar-Zapol'skiy) and Polish botanists K. Filipowicz and F. Błoński (Błoński 1888, 1889; Downar 1861; Filipowicz 1881; Gilibert 1781, 1792). In the early 20th century (1900–1925), there was a second phase of lichenological discovery in Belarus. During that time, Belarusian pioneer lichenologist V.P. Savicz and his wife L.I. Ljubitzkaja (later Savicz-Ljubitzkaja) reported 91 species new to the country (Ljubitzkaja 1914; Savicz 1909, 1910, 1911, 1925; Savicz & Savicz 1924; Wyssotzky et al.