Lichen-Forming and Lichenicolous Fungi New to Kazakhstan
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Research Journal of Pharmaceutical, Biological and Chemical Sciences
ISSN: 0975-8585 Research Journal of Pharmaceutical, Biological and Chemical Sciences Population Studies of Hedysarum theinum Krasnob. At the Ivanovsky Mountain Range of The Kazakh Altai Mountains. Alevtina Nikolaevna Danilova*, Yuri Andreevich Kotukhov, Olga Alexandrovna Anufrieva, and Serik Argynbekovich Kubentayev. Republican state enterprise "Altai Botanical Garden" of the Committee of Science, Ministry of Education and Science of the Republic of Kazakhstan 071300, Republic of Kazakhstan, East Kazakhstan Region, Ridder, Ermakova str., 1 ABSTRACT The current paper represents ecological, biological, and resource studies of Hedysarum theinum Krasnob. at the Ivanovsky Mountain Range of the Kazakh Altai Mountains. We have provided a phytocoenotic description of the species’ habitat, and determined the ontogenesis, age composition of the coenopopulations, numbers, presence of pests and pathogenic organisms, as well as the seasonal rhythm of development of sweetvetch. We have found that Hedysarum theinum inhabits large territories of the Ivanovsky Mountain Range and undergoes excessive anthropogenic impact. The species does not form industrial reserves and may serve as a source of raw materials for the local pharmacy chain. Within the coenopopulations, the species acts as dominant or subdominant. The sweetvetch coenopopulations from different sites of the Ivanovsky Mountain Range have similar age composition with uniform age spectra: in all cases the absolute maxima account for mature reproductive individuals. The populations of this species have normal age distributions lacking certain stages, they are dominated by mature generative plants, the numbers of juvenile and premature individuals are low, whereas senile plants are completely absent. Seed productivity undergoes substantial fluctuations over the years, also depending on the altitude of the species’ habitat and climatic conditions during the vegetative period, while almost all altitudinal belts are marked by relatively high seed productivity. -
Romanian Journal of Biology1 Plant Biology
ROMANIAN JOURNAL OF BIOLOGY1 PLANT BIOLOGY VOLUMES 59–60 2014–2015 CONTENTS C. MAXIMILIAN, I. HOLOBIUC, L. JIANU, A. BREZEANU, In vitro callus production in the medicinal, rare and endangered species Ecballium elaterium (L.) A. Richard ............................................................................. 3 R. THAPAR KAPOOR, Evaluation of insecticidal potential of root extracts of Rauvolfia tetraphylla against Musca domestica ............................................ 15 M. THIRUPATHI REDDY, K. HARIBABU, M. GANESH, K. CHANDRASEKHAR REDDY, H. BEGUM, J. DILIP BABU, R. S. KRISHNA REDDY, B. PURUSHOTHAMA REDDY, G. NARSHIMULU, Genetic variability for growth, earliness and yield attributes in okra (Abelmoschus esculentus (L.) Moench) ............................ 27 I. VICOL, Chorology of Mycarthopyrenia KEISSL genus in Romania ................... 41 S. M. MOHSIN, R. ISLAM MD, A. ABU NOMAN FARUQ, H.A.C. NISHA, R. S. BORNA, M. N. ISLAM, The genetic variability of Alternaria porri in Bangladesh .............................................................................................. 47 H OLOUMI., F. NASERI, R. SOLTANINEJAD, Comparative study of essential oil chemical constituents of Calotropis procera leaves collected from different natural localities ............................................................................. 59 1 ROM. J. BIOL. – PLANT BIOL., VOLUMEs 59–60, P. 1–68, BUCHAREST, 2014–2015 IN VITRO CALLUS PRODUCTION IN THE MEDICINAL, RARE AND ENDANGERED SPECIES ECBALLIUM ELATERIUM (L.) A. RICHARD CARMEN MAXIMILIAN1*, -
First Record of Mycoporum Buckii (Dothideomycetes, Pleosporales) in Mexico Primer Registro De Mycoporum Buckii (Dothideomycetes, Pleosporales) En México
Scientific note First record of Mycoporum buckii (Dothideomycetes, Pleosporales) in Mexico Primer registro de Mycoporum buckii (Dothideomycetes, Pleosporales) en México Yenitze A. García-Martínez1 , Gabriela Heredia2 , Ricardo Valenzuela1 , Tania Raymundo1,3 Abstract Background and Aims: The genus Mycoporum of the class Dothideomycetes of the phylum Ascomycota is characterised by ascostromata with scattered, aggregated locules without a wall of their own, bitunicate asci with a short pedicel, as well as ellipsoidal, fusiform to clavate ascospores with broader upper hemispores, and a variable number of septa. The objective of this study is to reportMycoporum buckii for the first time in Mexico. Methods: The specimens were collected on Rhizophora mangle bark in the Cozumel Island Biosphere Reserve, Quintana Roo, Mexico, in 2019, and were deposited in the herbarium ENCB of the Instituto Politécnico Nacional, Mexico. The material was reviewed in dry state, and macro- and micro- morphological characters were described. Specimens were identified with specialised keys and literature. Key results: The description of Mycoporum buckii of Mexico is presented. This species is characterised by multilocular, sessile ascostromata, clavate asci, and ellipsoidal ascospores with one transversal septum. Conclusions: Mycoporum buckii grows on Rhizophora mangle and produces its sporomas during the rainy and dry seasons in the Cozumel Island Biosphere Reserve, Quintana Roo, Mexico. Key words: Caribbean Sea, Rhizophora mangle, taxonomy. Resumen Antecedentes y Objetivos: El género Mycoporum de la clase Dothideomycetes del phylum Ascomycota se caracteriza por un ascostroma con lóculos dispersos, agregados sin pared propia, ascas bitunicadas con un pedicelo corto y ascoporas elipsoidales, fusiformes a clavadas, con el hemisferio superior más ancho, y un numero variable de septos. -
Domenico Puntillo & Sonia Ravera Naetrocymbe Mori
Fl. Medit. 23: 5-9 doi: 10.7320/FlMedit23.005 Version of Record published online on 30 December 2013 Domenico Puntillo & Sonia Ravera Naetrocymbe mori-albae, a new species from Calabria (Southern Italy) Abstract Puntillo, D. & Ravera S.: Naetrocymbe mori-albae, a new species from Calabria (Southern Italy). — Fl. Medit. 23: 5-9. 2013. — ISSN: 1120-4052 printed, 2240-4538 online. The new taxon belongs to the group Arthopyrenia rhyponta-A. punctiformis, recently trans- ferred to the problematic genus Naetrocymbe Korb. (Naetrocymbaceae Höhn. ex R.C. Harris), as it is a non or weakly lichenized group. This species is characterized by tadpole-shaped 1-sep- tate ascospores with a conical lower cell and perithecia which are 4-8 linearly arranged. Key words: Naetrocymbe, Lichenes, Italy. Introduction Naetrocymbe is a genus of pyrenocarpous ascomycetes belonging to the family Naetrocymbaceae establish by Harris (1995). This family includes species usually not lichen-forming and characterized by short-celled paraphyses with refractive bodies near the septa, obpyriform asci with a distinctive apical region lacking a nasse and short rod- shaped microconidia. It has a mainly temperate/boreal distribution. Because of some Naetrocymbe species can be lichenized (Keissler 1938; Knudsen & Lendemer 2009; Roux 2009), Aptroot (1998, 2002), Coppins (2002) and Coppins & Orange (2009) consider unnecessary a separation between Naetrocymbe and Arthopyrenia. They disagree with Harris (1973, 1975, 1995), Tucker & Harris (1980) and Coppins (1988), about the impor- tance of the hamathecial tissues as valuable character. In Aptroot’s opinion, the cosmopol- itan genus Arthopyrenia s.l. should be considered in its original wide concept: character- ized by branched pseudoparaphyses, which may disappear, and sole-shaped ascospores. -
Mycosphere Notes 225–274: Types and Other Specimens of Some Genera of Ascomycota
Mycosphere 9(4): 647–754 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/4/3 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Notes 225–274: types and other specimens of some genera of Ascomycota Doilom M1,2,3, Hyde KD2,3,6, Phookamsak R1,2,3, Dai DQ4,, Tang LZ4,14, Hongsanan S5, Chomnunti P6, Boonmee S6, Dayarathne MC6, Li WJ6, Thambugala KM6, Perera RH 6, Daranagama DA6,13, Norphanphoun C6, Konta S6, Dong W6,7, Ertz D8,9, Phillips AJL10, McKenzie EHC11, Vinit K6,7, Ariyawansa HA12, Jones EBG7, Mortimer PE2, Xu JC2,3, Promputtha I1 1 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, China 3 World Agro Forestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan Province, People’s Republic of China 4 Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China 5 Shenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China 6 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 7 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 8 Department Research (BT), Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium 9 Direction Générale de l'Enseignement non obligatoire et de la Recherche scientifique, Fédération Wallonie-Bruxelles, Rue A. -
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. -
BLS Bulletin 111 Winter 2012.Pdf
1 BRITISH LICHEN SOCIETY OFFICERS AND CONTACTS 2012 PRESIDENT B.P. Hilton, Beauregard, 5 Alscott Gardens, Alverdiscott, Barnstaple, Devon EX31 3QJ; e-mail [email protected] VICE-PRESIDENT J. Simkin, 41 North Road, Ponteland, Newcastle upon Tyne NE20 9UN, email [email protected] SECRETARY C. Ellis, Royal Botanic Garden, 20A Inverleith Row, Edinburgh EH3 5LR; email [email protected] TREASURER J.F. Skinner, 28 Parkanaur Avenue, Southend-on-Sea, Essex SS1 3HY, email [email protected] ASSISTANT TREASURER AND MEMBERSHIP SECRETARY H. Döring, Mycology Section, Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, email [email protected] REGIONAL TREASURER (Americas) J.W. Hinds, 254 Forest Avenue, Orono, Maine 04473-3202, USA; email [email protected]. CHAIR OF THE DATA COMMITTEE D.J. Hill, Yew Tree Cottage, Yew Tree Lane, Compton Martin, Bristol BS40 6JS, email [email protected] MAPPING RECORDER AND ARCHIVIST M.R.D. Seaward, Department of Archaeological, Geographical & Environmental Sciences, University of Bradford, West Yorkshire BD7 1DP, email [email protected] DATA MANAGER J. Simkin, 41 North Road, Ponteland, Newcastle upon Tyne NE20 9UN, email [email protected] SENIOR EDITOR (LICHENOLOGIST) P.D. Crittenden, School of Life Science, The University, Nottingham NG7 2RD, email [email protected] BULLETIN EDITOR P.F. Cannon, CABI and Royal Botanic Gardens Kew; postal address Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, email [email protected] CHAIR OF CONSERVATION COMMITTEE & CONSERVATION OFFICER B.W. Edwards, DERC, Library Headquarters, Colliton Park, Dorchester, Dorset DT1 1XJ, email [email protected] CHAIR OF THE EDUCATION AND PROMOTION COMMITTEE: S. -
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. -
New Records of One <I>Amygdalaria</I> and Three <I
ISSN (print) 0093-4666 © 2015. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/130.33 Volume 130, pp. 33–40 January–March 2015 New records of one Amygdalaria and three Porpidia taxa (Lecideaceae) from China Lu-Lu Zhang, Xin Zhao, & Ling Hu * Key Laboratory of Plant Stress Research, College of Life Sciences, Shandong Normal University, Jinan, 250014, P. R. China * Correspondence to: [email protected] Abstract —Four lichen taxa of Lecideaceae, Amygdalaria consentiens var. consentiens, Porpidia carlottiana, P. lowiana, and P. tuberculosa, are reported for the first time from China. Key words —Asia, Lecideales, lichens Introduction The family Lecideaceae Chevall. contains about 23 genera and 547 species, of which the largest genus is Lecidea Ach., containing about 427 species (Kirk et al. 2008, Fryday & Hertel 2014). In China, twenty-three species of the other genera in Lecideaceae have been reported, including two each of Amygdalaria Norman, Bellemerea Hafellner & Cl. Roux, and Immersaria Rambold & Pietschm.; one each of Lecidoma Gotth. Schneid. & Hertel, Paraporpidia Rambold & Pietschm., and Stenhammarella Hertel; and 16 species of Porpidia Körb. (Hertel 1977, Wei 1991; Aptroot & Seaward 1999; Aptroot 2002; Aptroot & Sparrius 2003; Obermayer 2004; Guo 2005; Zhang et al. 2010, 2012; Wang et al. 2012; Ismayi & Abbas 2013; Hu et al. 2014). Amygdalaria and Porpidia are obviously very closely related. Both have large halonate ascospores, a high hymenium, Porpidia-type asci, and a dark pigmented hypothecium and are (with a few exceptions) restricted to lime-free, silicate rocks. However Amygdalaria can be best distinguished from Porpidia by the presence of cephalodia, the higher hymenium (over 130 µm), the larger ascospores (generally 20–35 × 10–16 µm) with conspicuous, rather compact epispores, and a tendency toward a brownish or yellowish pink thallus (Inoue 1984, Brodo & Hertel 1987, Gowan 1989, Smith et al. -
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). -
<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 -
Malus Sieversii Belongs to the Rose Family, Rosaceae (Making It Related to Other Fruit Trees, Including Apricots, Plums, Cherries and Almonds)
| REPORT © Georgy Georgy Lazkov - Malus sieversii – wild apple wild FAUNA & FLORA INTERNATIONAL’S М a l u s s i e v e r s i i – w i l d a p p l e : s p e c i e s s t a t u s review and action plan for its conservation in Childukhtaron a n d D a s h t i j u m r e s e r v e s , T a j i k i s t a n |PREPARED BY: Gulazor Miravalova, FFI Intern David Gill, Programme Manager, Central Asia, FFI Mario Boboev, Director of Kulob Botanical Garden Rasima Sabzalieva, Project Assistant, FFI Tajikistan April 2020 Мalus sieversii – wild apple: species status review and action plan for its conservation in Childukhtaron and Dashtijum reserves, Tajikistan Written by: Gulazor Miravalova, FFI Intern Edited by: David Gill, Programme Manager, Central Asia, FFI Mario Boboev, Director of Kulob Botanical Garden Rasima Sabzalieva, Project Assistant, FFI Tajikistan Photo credit: Mario Boboev April 2020 2 Table of contents 1. SPECIES DESCRIPTION ............................................................................................... 4 1.1.TAXONOMY .................................................................................................................... 4 1.2 STATUS .......................................................................................................................... 4 1.3. BIOLOGY/ DESCRIPTION ................................................................................................. 4 2. CURRENT DISTRIBUTION............................................................................................. 6 2.1.GLOBAL ........................................................................................................................