Lodgepole Pine (Pinus Contorta Douglas Ex Loudon) from the Perspective of Its Possible Utilization in Conditions of Changing Central European Climate
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Patellariaceae Revisited
Mycosphere 6 (3): 290–326(2015) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2015 Online Edition Doi 10.5943/mycosphere/6/3/7 Patellariaceae revisited Yacharoen S1,2, Tian Q1,2, Chomnunti P1,2, Boonmee S1, Chukeatirote E2, Bhat JD3 and Hyde KD1,2,4,5* 1Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 2School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3Formerly at Department of Botany, Goa University, Goa 403 206, India 4Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 5World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, China Yacharoen S, Tian Q, Chomnunti P, Boonmee S, Chukeatirote E, Bhat JD, Hyde KD 2015 – Patellariaceae revisited. Mycosphere 6(3), 290–326, Doi 10.5943/mycosphere/6/3/7 Abstract The Dothideomycetes include several genera whose ascomata can be considered as apothecia and thus would be grouped as discomycetes. Most genera are grouped in the family Patellariaceae, but also Agrynnaceae and other families. The Hysteriales include genera having hysterioid ascomata and can be confused with species in Patellariaceae with discoid apothecia if the opening is wide enough. In this study, genera of the family Patellariaceae were re-examined and characterized based on morphological examination. As a result of this study the genera Baggea, Endotryblidium, Holmiella, Hysteropatella, Lecanidiella, Lirellodisca, Murangium, Patellaria, Poetschia, Rhizodiscina, Schrakia, Stratisporella and Tryblidaria are retained in the family Patellariaceae. The genera Banhegyia, Pseudoparodia and Rhytidhysteron are excluded because of differing morphology and/or molecular data. -
Biodiversity Climate Change Impacts Report Card Technical Paper 12. the Impact of Climate Change on Biological Phenology In
Sparks Pheno logy Biodiversity Report Card paper 12 2015 Biodiversity Climate Change impacts report card technical paper 12. The impact of climate change on biological phenology in the UK Tim Sparks1 & Humphrey Crick2 1 Faculty of Engineering and Computing, Coventry University, Priory Street, Coventry, CV1 5FB 2 Natural England, Eastbrook, Shaftesbury Road, Cambridge, CB2 8DR Email: [email protected]; [email protected] 1 Sparks Pheno logy Biodiversity Report Card paper 12 2015 Executive summary Phenology can be described as the study of the timing of recurring natural events. The UK has a long history of phenological recording, particularly of first and last dates, but systematic national recording schemes are able to provide information on the distributions of events. The majority of data concern spring phenology, autumn phenology is relatively under-recorded. The UK is not usually water-limited in spring and therefore the major driver of the timing of life cycles (phenology) in the UK is temperature [H]. Phenological responses to temperature vary between species [H] but climate change remains the major driver of changed phenology [M]. For some species, other factors may also be important, such as soil biota, nutrients and daylength [M]. Wherever data is collected the majority of evidence suggests that spring events have advanced [H]. Thus, data show advances in the timing of bird spring migration [H], short distance migrants responding more than long-distance migrants [H], of egg laying in birds [H], in the flowering and leafing of plants[H] (although annual species may be more responsive than perennial species [L]), in the emergence dates of various invertebrates (butterflies [H], moths [M], aphids [H], dragonflies [M], hoverflies [L], carabid beetles [M]), in the migration [M] and breeding [M] of amphibians, in the fruiting of spring fungi [M], in freshwater fish migration [L] and spawning [L], in freshwater plankton [M], in the breeding activity among ruminant mammals [L] and the questing behaviour of ticks [L]. -
Panolis Flammea (Denis & Schiffermüller)
Pine Beauty Screening Aid Panolis flammea (Denis & Schiffermüller) Todd M. Gilligan1 and Steven C. Passoa2 1) Identification Technology Program (ITP) / Colorado State University, USDA-APHIS-PPQ-Science & Technology (S&T), 2301 Research Boulevard, Suite 108, Fort Collins, Colorado 80526 U.S.A. (Email: [email protected]) 2) USDA-APHIS-PPQ, The Ohio State University and USDA Forest Service Northern Research Station, 1315 Kinnear Road, Columbus, Ohio 43212 U.S.A. (Email: [email protected]) This CAPS (Cooperative Agricultural Pest Survey) screening aid produced for and distributed by: Version 2.0 USDA-APHIS-PPQ National Identification Services (NIS) 30 Jun 2014 This and other identification resources are available at: http://caps.ceris.purdue.edu/taxonomic_services The pine beauty, Panolis flammea (Denis & Schiffermüller), is a serious pest of Pinaceae in Europe. Larvae have been recorded on Douglas-fir, fir, juniper, larch, pine (lodgepole pine, Scots pine), and spruce. Early instar larvae feed inside the needles of new growth and later instars feed on older foliage. Outbreaks of P. flammea in pine plantations in the United Kingdom and Continental Europe have caused damage to thousands of acres and resulted in significant tree mortality. In the UK, adults are present from March through May. Twenty to eighty year old pine monocultures are especially at risk, and lodgepole pine, common in the western U.S., has been attacked when planted in Scotland (see Bradshaw et al. 1983; Sukovata et al. 2003). Panolis flammea is a member of the Noctuidae (tribe Hadenini), the family of moths (Lepidoptera) with the largest number of total species and also the most pest species. -
Fungal Diversity in the Mediterranean Area
Fungal Diversity in the Mediterranean Area • Giuseppe Venturella Fungal Diversity in the Mediterranean Area Edited by Giuseppe Venturella Printed Edition of the Special Issue Published in Diversity www.mdpi.com/journal/diversity Fungal Diversity in the Mediterranean Area Fungal Diversity in the Mediterranean Area Editor Giuseppe Venturella MDPI • Basel • Beijing • Wuhan • Barcelona • Belgrade • Manchester • Tokyo • Cluj • Tianjin Editor Giuseppe Venturella University of Palermo Italy Editorial Office MDPI St. Alban-Anlage 66 4052 Basel, Switzerland This is a reprint of articles from the Special Issue published online in the open access journal Diversity (ISSN 1424-2818) (available at: https://www.mdpi.com/journal/diversity/special issues/ fungal diversity). For citation purposes, cite each article independently as indicated on the article page online and as indicated below: LastName, A.A.; LastName, B.B.; LastName, C.C. Article Title. Journal Name Year, Article Number, Page Range. ISBN 978-3-03936-978-2 (Hbk) ISBN 978-3-03936-979-9 (PDF) c 2020 by the authors. Articles in this book are Open Access and distributed under the Creative Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. The book as a whole is distributed by MDPI under the terms and conditions of the Creative Commons license CC BY-NC-ND. Contents About the Editor .............................................. vii Giuseppe Venturella Fungal Diversity in the Mediterranean Area Reprinted from: Diversity 2020, 12, 253, doi:10.3390/d12060253 .................... 1 Elias Polemis, Vassiliki Fryssouli, Vassileios Daskalopoulos and Georgios I. -
Preliminary Classification of Leotiomycetes
Mycosphere 10(1): 310–489 (2019) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/10/1/7 Preliminary classification of Leotiomycetes Ekanayaka AH1,2, Hyde KD1,2, Gentekaki E2,3, McKenzie EHC4, Zhao Q1,*, Bulgakov TS5, Camporesi E6,7 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 4Landcare Research Manaaki Whenua, Private Bag 92170, Auckland, New Zealand 5Russian Research Institute of Floriculture and Subtropical Crops, 2/28 Yana Fabritsiusa Street, Sochi 354002, Krasnodar region, Russia 6A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy. 7A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314 Brescia, Italy. Ekanayaka AH, Hyde KD, Gentekaki E, McKenzie EHC, Zhao Q, Bulgakov TS, Camporesi E 2019 – Preliminary classification of Leotiomycetes. Mycosphere 10(1), 310–489, Doi 10.5943/mycosphere/10/1/7 Abstract Leotiomycetes is regarded as the inoperculate class of discomycetes within the phylum Ascomycota. Taxa are mainly characterized by asci with a simple pore blueing in Melzer’s reagent, although some taxa have lost this character. The monophyly of this class has been verified in several recent molecular studies. However, circumscription of the orders, families and generic level delimitation are still unsettled. This paper provides a modified backbone tree for the class Leotiomycetes based on phylogenetic analysis of combined ITS, LSU, SSU, TEF, and RPB2 loci. In the phylogenetic analysis, Leotiomycetes separates into 19 clades, which can be recognized as orders and order-level clades. -
Pseudodiplodia Cenangiicola Sp. Nov., a Fungus on Cenangium Ferruginosum
Karsienia i9: 30-Ji. 1979 Pseudodiplodia cenangiicola sp. nov., a fungus on Cenangium ferruginosum D.W. MINTER MINTER, D.W. 1979: Pseudodiplodia cenangiicola sp. nov., a fungus on Cenangium ferruginosum. - Karstenia 19: 30- 31. A new coelomycete, Pseudodiplodia cenangiicola Nevodovsky ex Minter, on ascocarps of Cenangium ferruginosum Fr. ex Fr. (a fungus inhabiting pine twigs) is described from Krasnoyarsk, Siberia. D. W. Minter, Commonwealth Mycological Institute, Ferry Lane, Kew, Surrey, England Cenangium ferruginosum Fr. ex Fr. (Ascomycetes, Botanical Nomenclature relevant. This states that Helotiales) is a common saprophyte on twigs of 'the distribution on or after 1 Jan. 1953 of printed pines. Collections in the herbaria of the Royal matter accompanying exsiccata does not constitute Botanic Gardens, Kew (K) and the Commonwealth effective publication', with the proviso that 'if the Mycological Institute, Kew (IMI) were recently printed matter is also distributed independently of the examined and two specimens of an unusual collection exsiccata, this constitutes effective publication'. from Krasnoyarsk (Siberia, U.S.S.R.) in October Unless the terms of the proviso were met, therefore, 1950 were discovered. They were labelled as Microdiplodia cenangiicola was not effectively, and Cenangium abietis (Pers.) Rehm (a synonym of C. hence not validly published. Examination of corre ferruginosum), and formed no. 29 of the second spondence files at C.M.I. revealed that in 1956 an fascicle of the exsiccata 'Griby SSSR', published in enquiry was made concerning the validity of other Moscow in 1954. On the label was included a Latin names published in the first fascicle of this series of description of a new species, Microdiplodia exsiccata. -
Field Identification Guide Pine Processionary Moth
Field Identification Guide Pine processionary moth Photograph: Mat Holloway, Observatree volunteer Observatree Holloway, Mat Photograph: Funded by the EU’s LIFE programme Pine processionary moth The caterpillars (larvae) of the pine processionary moth (PPM) (Thaumetopoea pityocampa) can threaten the health of pine trees (Pinus species) by feeding on their needles. Large populations cause extensive defoliation of pine trees, leaving them vulnerable to attack by other pests and diseases, and less able to withstand adverse environmental events such as floods and droughts. Timber production and tree growth can be reduced as a result of attack. The caterpillars are also a significant public and animal health risk, as they bear toxic hairs which can cause itching skin rashes, eye and throat irritation and breathing problems. Hence it is important not to approach or touch the caterpillars, or their nests. Species affected The main hosts for PPM are pine trees with our native Scots pine (Pinus sylvestris) and the widely planted Corsican pine (P. nigra ssp. laricio) being at the greatest risk from this pest in the UK. Other species that are susceptible include the Aleppo pine (P. halepensis), Austrian pine (P. nigra), Canary Island pine (P. canariensis), lodgepole pine (P. contorta), maritime pine (P. pinaster), Monterey pine (P. radiata) and stone pine (P. pinea). The Atlas cedar (Cedrus atlantica) and European larch (Larix decidua) are also occasionally attacked. Signs and The main indicator of PPM attack is the presence of nests symptoms that are constructed by the caterpillars amongst the branches and foliage of pine trees. The caterpillars start to build the nests shortly after hatching. -
Diversity and Communities of Fungal Endophytes from Four Pi‐ Nus Species in Korea
Supplementary materials Diversity and communities of fungal endophytes from four Pi‐ nus species in Korea Soon Ok Rim 1, Mehwish Roy 1, Junhyun Jeon 1, Jake Adolf V. Montecillo 1, Soo‐Chul Park 2 and Hanhong Bae 1,* 1 Department of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Republic of Korea 2 Crop Biotechnology Institute, Green Bio Science & Technology, Seoul National University, Pyeongchang, Kangwon 25354, Republic of Korea * Correspondence: [email protected]; tel: 8253‐810‐3031 (office); Fax: 8253‐810‐4769 Keywords: host specificity; fungal endophyte; fungal diversity; pine trees Table S1. Characteristics and conditions of 18 sampling sites in Korea. Ka Ca Mg Precipitation Temperature Organic Available Available Geographic Loca‐ Latitude Longitude Altitude Tree Age Electrical Con‐ pine species (mm) (℃) pH Matter Phosphate Silicic acid tions (o) (o) (m) (years) (cmol+/kg) dictivity 2016 2016 (g/kg) (mg/kg) (mg/kg) Ansung (1R) 37.0744580 127.1119200 70 45 284 25.5 5.9 20.8 252.4 0.7 4.2 1.7 0.4 123.2 Seosan (2R) 36.8906971 126.4491716 60 45 295.6 25.2 6.1 22.3 336.6 1.1 6.6 2.4 1.1 75.9 Pinus rigida Jungeup (3R) 35.5521138 127.0191565 240 45 205.1 27.1 5.3 30.4 892.7 1.0 5.8 1.9 0.2 7.9 Yungyang(4R) 36.6061179 129.0885334 250 43 323.9 23 6.1 21.4 251.2 0.8 7.4 2.8 0.1 96.2 Jungeup (1D) 35.5565492 126.9866204 310 50 205.1 27.1 5.3 30.4 892.7 1.0 5.8 1.9 0.2 7.9 Jejudo (2D) 33.3737599 126.4716048 1030 40 98.6 27.4 5.3 50.6 591.7 1.2 4.6 1.8 1.7 0.0 Pinus densiflora Hoengseong (3D) 37.5098629 128.1603840 540 45 360.1 -
A Taxonomic and Phylogenetic Investigation of Conifer Endophytes
A Taxonomic and Phylogenetic Investigation of Conifer Endophytes of Eastern Canada by Joey B. Tanney A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology Carleton University Ottawa, Ontario © 2016 Abstract Research interest in endophytic fungi has increased substantially, yet is the current research paradigm capable of addressing fundamental taxonomic questions? More than half of the ca. 30,000 endophyte sequences accessioned into GenBank are unidentified to the family rank and this disparity grows every year. The problems with identifying endophytes are a lack of taxonomically informative morphological characters in vitro and a paucity of relevant DNA reference sequences. A study involving ca. 2,600 Picea endophyte cultures from the Acadian Forest Region in Eastern Canada sought to address these taxonomic issues with a combined approach involving molecular methods, classical taxonomy, and field work. It was hypothesized that foliar endophytes have complex life histories involving saprotrophic reproductive stages associated with the host foliage, alternative host substrates, or alternate hosts. Based on inferences from phylogenetic data, new field collections or herbarium specimens were sought to connect unidentifiable endophytes with identifiable material. Approximately 40 endophytes were connected with identifiable material, which resulted in the description of four novel genera and 21 novel species and substantial progress in endophyte taxonomy. Endophytes were connected with saprotrophs and exhibited reproductive stages on non-foliar tissues or different hosts. These results provide support for the foraging ascomycete hypothesis, postulating that for some fungi endophytism is a secondary life history strategy that facilitates persistence and dispersal in the absence of a primary host. -
Bulgariella Pulla, a Leotiomycete of Uncertain Placement, with an Uncommon Type of Ascus Opening
Mycologia ISSN: 0027-5514 (Print) 1557-2536 (Online) Journal homepage: http://www.tandfonline.com/loi/umyc20 Bulgariella pulla, a Leotiomycete of uncertain placement, with an uncommon type of ascus opening Teresa Iturriaga, Katherine F. LoBuglio & Donald H. Pfister To cite this article: Teresa Iturriaga, Katherine F. LoBuglio & Donald H. Pfister (2017) Bulgariella pulla, a Leotiomycete of uncertain placement, with an uncommon type of ascus opening, Mycologia, 109:6, 900-911, DOI: 10.1080/00275514.2017.1418590 To link to this article: https://doi.org/10.1080/00275514.2017.1418590 Accepted author version posted online: 09 Mar 2018. Published online: 14 Mar 2018. Submit your article to this journal Article views: 79 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=umyc20 MYCOLOGIA 2017, VOL. 109, NO. 6, 900–911 https://doi.org/10.1080/00275514.2017.1418590 Bulgariella pulla, a Leotiomycete of uncertain placement, with an uncommon type of ascus opening Teresa Iturriaga a,b, Katherine F. LoBuglioa, and Donald H. Pfister a aFarlow Herbarium, Harvard University, 22 Divinity Avenue, Cambridge, Massachusetts 02138; bDepartamento Biología de Organismos, Universidad Simón Bolívar, Caracas, Venezuela ABSTRACT ARTICLE HISTORY Bulgariella pulla (Leotiomycetes) is redescribed with the addition of characters of the ascus, spores, Received 8 December 2016 and habitat that were previously unconsidered. The ascus dehiscence mechanism in Bulgariella is Accepted 14 December 2017 unusual among Leotiomycetes. In this genus, asci lack a pore and open by splitting to form valves. KEYWORDS α α Phylogenetic analyses of partial sequences of translation elongation factor 1- (TEF1- ), the second Ascus dehiscence; Helotiales; largest subunit of RNA polymerase II (RPB2), and the 18S and 28S nuc rRNA genes determined that Pezizomycotina; phylogeny; Bulgariella belongs within Leotiomycetes but without conclusive assignment to an order or family. -
The Nantucket Pine Tip Moth: Old Problems, New Research
Unitfxi States Department of The Nantucket Pine Tip IMoth: Agriculture Old Problems, New Research Forest Service Proceedings of an Informal Conference The Entomological Society of America, Annual Meeting Southern Research Station General Technical Atlanta, Georgia Report SRS-51 December 12-I 6, 1999 Cover: Nantucket pine tip moth adult. Photo by Julie C. Weatherby. DISCLAIMER The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. PESTICIDE PRECAUTIONARY STATEMENT This publication reports research involving pesticides. It does not contain recommendations for their use, nor does it imply that the uses discussed here have been registered. All uses of pesticides must be registered by appropriate State and/or Federal agencies before they can be recommended. CAUTION: Pesticides can be injurious to humans, domestic animals, desirable plants, and fish or other wildlife if they are not handled or applied properly. Use all herbicides selectively and carefully. Follow recommended practices for the disposal of surplus pesticides and their containers. Papers published in these proceedings were submitted by authors in electronic media. Editing was done to ensure a consistent format. Authors are responsible for content and accuracy of their individual papers. June 2002 Southern Research Station P.O. Box 2680 Asheville, NC 28802 The Nantucket Pine Tip Moth: Old Problems, New Research Proceedings of an Informal Conference The Entomological Society of America, Annual Meeting December 12-I 6, 1999 Atlanta, Georgia Edited by C. Wayne Berisford, Professor Department of Entomology University of Georgia Athens, GA 30602-2603, USA Donald M. -
Catalogue of Pheromones
Table of Contents List of pheromones 3–4 Calendar 5 Products 6 Pests 7–41 Nun moth 7 Gypsy moth 8 Larger pine shoot beetle 10 May bug 11 Striped ambrosia beetle 12 Fir engraver beetle 14 Small spruce bark beetle 15 European spruce bark beetle 17 Larch bark beetle 18 Sharp toothed bark beetle 20 Six-toothed bark beetle 21 Northern bark beetle 23 Western larch case-bearer 24 Codling moth 25 Winter moth 27 Six-toothed spruce bark beetle 29 Western corn rootworm 30 Pine beauty 32 Large pine weevil and spruce weevil 33 Larch tortrix 35 Bud moth 36 Oak pinhole borer 37 Rose tortrix 38 Summer fruit tortrix 39 Pine shoot moth 40 Green oak tortrix 41 Acknowledgements 43 Contact 44 2 Product Species Trap type Trap placement Periods of trap placement Pine and spruce stands over 20 years old, Until mid-July LYMODOR Nun moth IBL-1 in the same places every year LYMODOR Gypsy moth IBL-1 Deciduous stands and orchards Until the end of June Pine stands and stands End of February TOMODOR Larger pine shoot beetle IBL-3 with a large share of pine Stands with a large share of Mid-April MELOLODOR May bug IBL-5 deciduous trees, especially oaks Stands, piles of debarked wood End of March TRYPODOR Striped ambrosia beetle IBL-2, IBL-3 trunks, wood material depots Fir stands and stands with Turn of April and May CURODOR Fir engraver beetle IBL-2, IBL-3 a large share of fir Turn of July and August AMITODOR Small spruce bark beetle IBL-2, IBL-3 Spruce stands End of April and the second half of June Spruce stands and stands End of April and the second half of June