Quercus Robur and Quercus Petraea
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Quercus Cerris
Quercus cerris Quercus cerris in Europe: distribution, habitat, usage and threats D. de Rigo, C. M. Enescu, T. Houston Durrant, G. Caudullo Turkey oak (Quercus cerris L.) is a deciduous tree native to southern Europe and Asia Minor, and a dominant species in the mixed forests of the Mediterranean basin. Turkey oak is a representative of section Cerris, a particular section within the genus Quercus which includes species for which the maturation of acorns occurs in the second year. Quercus cerris L., commonly known as Turkey oak, is a large fast-growing deciduous tree species growing to 40 m tall with 1 Frequency a trunk up to 1.5-2 m diameter , with a well-developed root < 25% system2. It can live for around 120-150 years3. The bark is 25% - 50% 50% - 75% mauve-grey and deeply furrowed with reddish-brown or orange > 75% bark fissures4, 5. Compared with other common oak species, e.g. Chorology Native sessile oak (Quercus petraea) and pedunculate oak (Quercus Introduced robur), the wood is inferior, and only useful for rough work such as shuttering or fuelwood1. The leaves are dark green above and grey-felted underneath6; they are variable in size and shape but are normally 9-12 cm long and 3-5 cm wide, with 7-9 pairs of triangular lobes6. The leaves turn yellow to gold in late autumn and drop off or persist in the crown until the next spring, especially on young trees3. The twigs are long and pubescent, grey or olive-green, with lenticels. The buds, which are concentrated Large shade tree in agricultural area near Altamura (Bari, South Italy). -
Morphometric Leaf Variation in Oaks (Quercus) of Bolu, Turkey
Ann. Bot. Fennici 40: 233–242 ISSN 0003-3847 Helsinki 29 August 2003 © Finnish Zoological and Botanical Publishing Board 2003 Morphometric leaf variation in oaks (Quercus) of Bolu, Turkey Aydın Borazan & Mehmet T. Babaç Department of Biology, Abant |zzet Baysal University, Gölköy 14280 Bolu, Turkey (e-mail: [email protected], [email protected]) Received 16 Sep. 2002, revised version received 7 Jan. 2003, accepted 10 Jan. 2003 Borazan, A. & Babaç, M. T. 2003: Morphometric leaf variation in oaks (Quercus) of Bolu, Turkey. — Ann. Bot. Fennici 40: 233–242. Genus Quercus (Fagaceae) has a problematic taxonomy because of widespread hybridization between the infrageneric taxa. The pattern of morphological leaf varia- tion was evaluated for evidence of hybridization in Bolu, Turkey, since previous stud- ies suggested that in oaks leaf morphology is a good indicator of putative hybridiza- tion. Principal components analysis was applied to data sets of leaf characters from fi ve populations to describe variation in leaf morphology. Leaf characters analyzed in this study showed high degrees of variation as a result of hybridization between four taxa (Q. pubescens, Q. virgiliana, Q. petraea and Q. robur) of subgenus Quercus while Q. cerris as a member of subgenus Cerris was clearly separated from the others. Key words: hybridization, morphological leaf variation, principal components analy- sis, Quercus Introduction in regions of mild and warm temperate climates. Fossil leaves indicate that todayʼs several major In the northern hemisphere oaks (Quercus) are oak groups are at least 40 million years old. Gen- conspicuous members of the temperate decidu- eral distribution of fossil ancestors supports the ous, broad leaved forests. -
Species List
1 of 16 Claypits 20/09/2021 species list Group Taxon Common Name Earliest Latest Records acarine Aceria macrorhyncha 2012 2012 1 acarine Aceria nalepai 2018 2018 1 amphibian Bufo bufo Common Toad 2001 2018 6 amphibian Lissotriton helveticus Palmate Newt 2001 2018 5 amphibian Lissotriton vulgaris Smooth Newt 2001 2001 1 annelid Hirudinea Leech 2011 2011 1 bird Acanthis cabaret Lesser Redpoll 2013 2013 1 bird Acrocephalus schoenobaenus Sedge Warbler 2001 2011 2 bird Aegithalos caudatus Long-tailed Tit 2011 2014 2 bird Alcedo atthis Kingfisher 2020 2020 1 bird Anas platyrhynchos Mallard 2013 2018 4 bird Anser Goose 2011 2011 1 bird Ardea cinerea Grey Heron 2013 2013 1 bird Aythya fuligula Tufted Duck 2013 2014 1 bird Buteo buteo Buzzard 2013 2014 2 bird Carduelis carduelis Goldfinch 2011 2014 5 bird Chloris chloris Greenfinch 2011 2014 6 bird Chroicocephalus ridibundus Black-headed Gull 2014 2014 1 bird Coloeus monedula Jackdaw 2011 2013 2 bird Columba livia Feral Pigeon 2014 2014 1 bird Columba palumbus Woodpigeon 2011 2018 8 bird Corvus corax Raven 2020 2020 1 bird Corvus corone Carrion Crow 2011 2014 5 bird Curruca communis Whitethroat 2011 2014 4 bird Cyanistes caeruleus Blue Tit 2011 2014 6 bird Cygnus olor Mute Swan 2013 2014 4 bird Delichon urbicum House Martin 2011 2011 1 bird Emberiza schoeniclus Reed Bunting 2013 2014 2 bird Erithacus rubecula Robin 2011 2014 7 bird Falco peregrinus Peregrine 2013 2013 1 bird Falco tinnunculus Kestrel 2010 2020 3 bird Fringilla coelebs Chaffinch 2011 2014 7 bird Gallinula chloropus Moorhen 2013 -
Phytophthora Ramorum Sudden Oak Death Pathogen
NAME OF SPECIES: Phytophthora ramorum Sudden Oak Death pathogen Synonyms: Common Name: Sudden Oak Death pathogen A. CURRENT STATUS AND DISTRIBUTION I. In Wisconsin? 1. YES NO X 2. Abundance: 3. Geographic Range: 4. Habitat Invaded: 5. Historical Status and Rate of Spread in Wisconsin: 6. Proportion of potential range occupied: II. Invasive in Similar Climate YES NO X Zones United States: In 14 coastal California Counties and in Curry County, Oregon. In nursery in Washington. Canada: Nursery in British Columbia. Europe: Germany, the Netherlands, the United Kingdom, Poland, Spain, France, Belgium, and Sweden. III. Invasive in Similar Habitat YES X NO Types IV. Habitat Affected 1. Habitat affected: this disease thrives in cool, wet climates including areas in coastal California within the fog belt or in low- lying forested areas along stream beds and other bodies of water. Oaks associated with understory species that are susceptible to foliar infections are at higher risk of becoming infected. 2. Host plants: Forty-five hosts are regulated for this disease. These hosts have been found naturally infected by P. ramorum and have had Koch’s postulates completed, reviewed and accepted. Approximately fifty-nine species are associated with Phytophthora ramorum. These species are found naturally infected; P. ramorum has been cultured or detected with PCR but Koch’s postulates have not been completed or documented and reviewed. Northern red oak (Quercus rubra) is considered an associated host. See end of document for complete list of plant hosts. National Risk Model and Map shows susceptible forest types in the mid-Atlantic region of the United States. -
Quercus Robur (Fagaceae)
Quercus robur (Fagaceae) The map description EEBIO area The integrated map shows the distribution and changes in the areal’s boundaries of pedunculate oak (Quercus robur). Q. robur is the dominant forest- formative species in the belt of broadleaf and mixed 4 needleleaf-broadleaf forests in the plains of the European part of the former USSR (Sokolov et al. 1977). In the northern part of its areal Q. robur grows in river valleys. In the central part, it forms mixed forests with Picea abies; closer to the south – a belt of broadleaf forests where Q. robur dominates. At the areal’s south boundary it forms small (marginal) forests in ravines and flood-plains (Atlas of Areals and Resources… , 1976). Q. robur belongs to the thermophilic species. The low temperature bound of possible occurrence of oak forests is marked by an average annual of 2?C l (http://www.forest.ru – in Russian). Therefore, l l l l l l hypotretically, oak areal boundaries will shift along l ll l l l l l l l with the changes in the average annual temperature. l l l l l l l l l l l For Yearly map of averaged mean annual air l l l l l l l l l l l l l l l l l l lll temperature (Afonin A., Lipiyaynen K., Tsepelev V., l l l l l l l ll ll l l l 2005) see http://www.agroatlas.spb.ru Climate. l l l l l l l l l l l l l l l l Oak forests are of great importance for the water l l l l l ll l lll l l l l l l l l l l l l l l l l l l l regime and soil structure, especially on the steep l l l l l l l l l l l l l l l l l l l l l l l l l l l l l slopes of river valleys and in forest-poor areas. -
5 Fagaceae Trees
CHAPTER 5 5 Fagaceae Trees Antoine Kremerl, Manuela Casasoli2,Teresa ~arreneche~,Catherine Bod6n2s1, Paul Sisco4,Thomas ~ubisiak~,Marta Scalfi6, Stefano Leonardi6,Erica ~akker~,Joukje ~uiteveld', Jeanne ~omero-Seversong, Kathiravetpillai Arumuganathanlo, Jeremy ~eror~',Caroline scotti-~aintagne", Guy Roussell, Maria Evangelista Bertocchil, Christian kxerl2,Ilga porth13, Fred ~ebard'~,Catherine clark15, John carlson16, Christophe Plomionl, Hans-Peter Koelewijn8, and Fiorella villani17 UMR Biodiversiti Genes & Communautis, INRA, 69 Route d'Arcachon, 33612 Cestas, France, e-mail: [email protected] Dipartimento di Biologia Vegetale, Universita "La Sapienza", Piazza A. Moro 5,00185 Rome, Italy Unite de Recherche sur les Especes Fruitikres et la Vigne, INRA, 71 Avenue Edouard Bourlaux, 33883 Villenave d'Ornon, France The American Chestnut Foundation, One Oak Plaza, Suite 308 Asheville, NC 28801, USA Southern Institute of Forest Genetics, USDA-Forest Service, 23332 Highway 67, Saucier, MS 39574-9344, USA Dipartimento di Scienze Ambientali, Universitk di Parma, Parco Area delle Scienze 1lIA, 43100 Parma, Italy Department of Ecology and Evolution, University of Chicago, 5801 South Ellis Avenue, Chicago, IL 60637, USA Alterra Wageningen UR, Centre for Ecosystem Studies, P.O. Box 47,6700 AA Wageningen, The Netherlands Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA lo Flow Cytometry and Imaging Core Laboratory, Benaroya Research Institute at Virginia Mason, 1201 Ninth Avenue, Seattle, WA 98101, -
What Is a Tree in the Mediterranean Basin Hotspot? a Critical Analysis
Médail et al. Forest Ecosystems (2019) 6:17 https://doi.org/10.1186/s40663-019-0170-6 RESEARCH Open Access What is a tree in the Mediterranean Basin hotspot? A critical analysis Frédéric Médail1* , Anne-Christine Monnet1, Daniel Pavon1, Toni Nikolic2, Panayotis Dimopoulos3, Gianluigi Bacchetta4, Juan Arroyo5, Zoltán Barina6, Marwan Cheikh Albassatneh7, Gianniantonio Domina8, Bruno Fady9, Vlado Matevski10, Stephen Mifsud11 and Agathe Leriche1 Abstract Background: Tree species represent 20% of the vascular plant species worldwide and they play a crucial role in the global functioning of the biosphere. The Mediterranean Basin is one of the 36 world biodiversity hotspots, and it is estimated that forests covered 82% of the landscape before the first human impacts, thousands of years ago. However, the spatial distribution of the Mediterranean biodiversity is still imperfectly known, and a focus on tree species constitutes a key issue for understanding forest functioning and develop conservation strategies. Methods: We provide the first comprehensive checklist of all native tree taxa (species and subspecies) present in the Mediterranean-European region (from Portugal to Cyprus). We identified some cases of woody species difficult to categorize as trees that we further called “cryptic trees”. We collected the occurrences of tree taxa by “administrative regions”, i.e. country or large island, and by biogeographical provinces. We studied the species-area relationship, and evaluated the conservation issues for threatened taxa following IUCN criteria. Results: We identified 245 tree taxa that included 210 species and 35 subspecies, belonging to 33 families and 64 genera. It included 46 endemic tree taxa (30 species and 16 subspecies), mainly distributed within a single biogeographical unit. -
Diagnosis of Phytophthora Ramorum in Trees
Diagnosis of PhytophthoraPhytophthora ramorumramorum in Trees by Dr. Kim D. Coder, Warnell School of Forest Resources, University of Georgia April, 2004 The organism shown to be responsible for SOD (sudden oak death) is Phytophthora ramorum, a fungus / yeast-like brown algae. This pathogen generates a number of symptoms in the trees infected. Of the trees and large shrubs shown to be infectable with this pathogen, some species have more serious stem and branch lesions like oaks, while other species have primarily leaf and twig lesions. In a single landscape, multiple hosts can keep the pathogen present for further attacks. This publication was prepared by reviewing approximately 35 research or disease announcement publications in Europe and North America. In addition, a number of factsheets and synthesized informa- tion guides were reviewed for continuity. This publication is designed for field diagnosis of SOD-like symptoms and related symptom sets on community trees. This publication should not be used in tree nursery situations, and is not a pathogen centered review. It is critical to seek pathological expertise and testing for confirming disease organism presence. A selected bibliography is available entitled “Sudden Oak Death – SOD: Bibliography of Important Literature.” (Coder, Kim D. 2004. University of Georgia, Warnell School of Forest Resources outreach publication SFR04-1. 2pp.). Names The tree syndrome or symptom set which characterizes attack by Phytophthora ramorum has common names of “ramorum dieback,” “ramorum blight,” “ramorum twig blight,”“ramorum leaf blight,” “ramorum stem canker,” “blood spot disease,” or “sudden oak death” (SOD). Phytophthora ramorum, and the less virulent Phytophthora nemorosa and Phytophthora pseudosyringae are all relatively new pathogen species recovered from trees which show ramorum blight symptoms. -
The Structure of Cynipid Oak Galls: Patterns in the Evolution of an Extended Phenotype
The structure of cynipid oak galls: patterns in the evolution of an extended phenotype Graham N. Stone1* and James M. Cook2 1Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK ([email protected]) 2Department of Biology, Imperial College, Silwood Park, Ascot, Berkshire SL5 7PY, UK Galls are highly specialized plant tissues whose development is induced by another organism. The most complex and diverse galls are those induced on oak trees by gallwasps (Hymenoptera: Cynipidae: Cyni- pini), each species inducing a characteristic gall structure. Debate continues over the possible adaptive signi¢cance of gall structural traits; some protect the gall inducer from attack by natural enemies, although the adaptive signi¢cance of others remains undemonstrated. Several gall traits are shared by groups of oak gallwasp species. It remains unknown whether shared traits represent (i) limited divergence from a shared ancestral gall form, or (ii) multiple cases of independent evolution. Here we map gall character states onto a molecular phylogeny of the oak cynipid genus Andricus, and demonstrate three features of the evolution of gall structure: (i) closely related species generally induce galls of similar structure; (ii) despite this general pattern, closely related species can induce markedly di¡erent galls; and (iii) several gall traits (the presence of many larval chambers in a single gall structure, surface resins, surface spines and internal air spaces) of demonstrated or suggested adaptive value to the gallwasp have evolved repeatedly. We discuss these results in the light of existing hypotheses on the adaptive signi¢cance of gall structure. Keywords: galls; Cynipidae; enemy-free space; extended phenotype; Andricus layers of woody or spongy tissue, complex air spaces within 1. -
Schematic Diagram of the Life Cycle of Agrilus Biguttatus on Native Oak Trees in Britain - from Egg to Adult
Forest Research Schematic diagram of the life cycle of Agrilus biguttatus on native oak trees in Britain - from egg to adult Sandra Denman and Nathan Brown, Forest Research As temperatures warm up, larvae continue to feed and grow, in widening galleries. As larvae ‘outgrow’ their skin they go through a moulting phase Early instar larvae enter Year 1 continued to a bigger size or ‘instar’. The fi rst overwintering period larvae go through 5 instar Feb M phases before pupation. n ar Ja A pr ec D M ay ov N Larvae approach Acute oak decline (AOD) is a condition of mature fully grown status native oak in Britain that appears to be increasing. 2 Aff ected trees are identifi ed by symptoms of t uly c J r a e profuse stem bleeding and signifi cant tree O y Larvae migrate to outer bark g Ju u n A o mortality. Two organisms are thought to play key e t Year 2 for 2nd overwintering, in pupal in g roles in AOD; bacteria and the buprestid beetle chamber in bark plate n i o g In warmer climates Agrilus biguttatus. This poster describes the life p e p development may S cycle of Agrilus biguttatus in Britian. e be completed in S Eggs hatch and larvae feed on one year O the cambial tissues creating c t sinuous galleries. N ov De A c u Ja Apr Females lay eggs in bark crevices g n F ar eb M Pupation takes place, adult ready for J emergence uly ay M START M year 1 id-en d June June Adults emerge Names Mating and egg laying begins Adult beetles feed on foliage in canopy. -
From Genes to Genomes: Botanic Gardens Embracing New Tools for Conservation and Research Volume 18 • Number 1
Journal of Botanic Gardens Conservation International Volume 18 • Number 1 • February 2021 From genes to genomes: botanic gardens embracing new tools for conservation and research Volume 18 • Number 1 IN THIS ISSUE... EDITORS Suzanne Sharrock EDITORIAL: Director of Global Programmes FROM GENES TO GENOMES: BOTANIC GARDENS EMBRACING NEW TOOLS FOR CONSERVATION AND RESEARCH .... 03 Morgan Gostel Research Botanist, FEATURES Fort Worth Botanic Garden Botanical Research Institute of Texas and Director, GGI-Gardens NEWS FROM BGCI .... 06 Jean Linksy FEATURED GARDEN: THE NORTHWESTERN UNIVERSITY Magnolia Consortium Coordinator, ECOLOGICAL PARK & BOTANIC GARDENS .... 09 Atlanta Botanical Garden PLANT HUNTING TALES: GARDENS AND THEIR LESSONS: THE JOURNAL OF A BOTANY STUDENT Farahnoz Khojayori .... 13 Cover Photo: Young and aspiring scientists assist career scientists in sampling plants at the U.S. Botanic Garden for TALKING PLANTS: JONATHAN CODDINGTON, the Global Genome Initiative (U.S. Botanic Garden). DIRECTOR OF THE GLOBAL GENOME INITIATIVE .... 16 Design: Seascape www.seascapedesign.co.uk BGjournal is published by Botanic Gardens Conservation International (BGCI). It is published twice a year. Membership is open to all interested individuals, institutions and organisations that support the aims of BGCI. Further details available from: ARTICLES • Botanic Gardens Conservation International, Descanso House, 199 Kew Road, Richmond, Surrey TW9 3BW UK. Tel: +44 (0)20 8332 5953, Fax: +44 (0)20 8332 5956, E-mail: [email protected], www.bgci.org BANKING BOTANICAL BIODIVERSITY WITH THE GLOBAL GENOME • BGCI (US) Inc, The Huntington Library, BIODIVERSITY NETWORK (GGBN) Art Collections and Botanical Gardens, Ole Seberg, Gabi Dröge, Jonathan Coddington and Katharine Barker .... 19 1151 Oxford Rd, San Marino, CA 91108, USA. -
National Oak Gall Wasp Survey
ational Oak Gall Wasp Survey – mapping with parabiologists in Finland Bess Hardwick Table of Contents 1. Introduction ................................................................................................................. 2 1.1. Parabiologists in data collecting ............................................................................. 2 1.2. Oak cynipid gall wasps .......................................................................................... 3 1.3. Motivations and objectives .................................................................................... 4 2. Material and methods ................................................................................................ 5 2.1. The volunteers ........................................................................................................ 5 2.2. Sampling ................................................................................................................. 6 2.3. Processing of samples ............................................................................................ 7 2.4. Data selection ........................................................................................................ 7 2.5. Statistical analyses ................................................................................................. 9 3. Results ....................................................................................................................... 10 3.1. Sampling success .................................................................................................