Chestnut Integrated Pest Management
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CHESTNUT (CASTANEA Spp.) CULTIVAR EVALUATION for COMMERCIAL CHESTNUT PRODUCTION
CHESTNUT (CASTANEA spp.) CULTIVAR EVALUATION FOR COMMERCIAL CHESTNUT PRODUCTION IN HAMILTON COUNTY, TENNESSEE By Ana Maria Metaxas Approved: James Hill Craddock Jennifer Boyd Professor of Biological Sciences Assistant Professor of Biological and Environmental Sciences (Director of Thesis) (Committee Member) Gregory Reighard Jeffery Elwell Professor of Horticulture Dean, College of Arts and Sciences (Committee Member) A. Jerald Ainsworth Dean of the Graduate School CHESTNUT (CASTANEA spp.) CULTIVAR EVALUATION FOR COMMERCIAL CHESTNUT PRODUCTION IN HAMILTON COUNTY, TENNESSEE by Ana Maria Metaxas A Thesis Submitted to the Faculty of the University of Tennessee at Chattanooga in Partial Fulfillment of the Requirements for the Degree of Master of Science in Environmental Science May 2013 ii ABSTRACT Chestnut cultivars were evaluated for their commercial applicability under the environmental conditions in Hamilton County, TN at 35°13ꞌ 45ꞌꞌ N 85° 00ꞌ 03.97ꞌꞌ W elevation 230 meters. In 2003 and 2004, 534 trees were planted, representing 64 different cultivars, varieties, and species. Twenty trees from each of 20 different cultivars were planted as five-tree plots in a randomized complete block design in four blocks of 100 trees each, amounting to 400 trees. The remaining 44 chestnut cultivars, varieties, and species served as a germplasm collection. These were planted in guard rows surrounding the four blocks in completely randomized, single-tree plots. In the analysis, we investigated our collection predominantly with the aim to: 1) discover the degree of acclimation of grower- recommended cultivars to southeastern Tennessee climatic conditions and 2) ascertain the cultivars’ ability to survive in the area with Cryphonectria parasitica and other chestnut diseases and pests present. -
Leafy and Crown Gall
Is it Crown Gall or Leafy Gall? Melodie L. Putnam and Marilyn Miller Humphrey Gifford, an early English poet said, “I cannot say the crow is white, But needs must call a spade a spade.” To call a thing by its simplest and best understood name is what is meant by calling a spade a spade. We have found confusion around the plant disease typified by leafy galls and shoot proliferation, and we want to call a spade a spade. The bacterium Rhodococcus fascians causes fasciation, leafy galls and shoot proliferation on plants. These symptoms have been attributed variously to crown gall bacteria (Agrobacterium tumefaciens), virus infection, herbicide damage, or eriophyid mite infestation. There is also confusion about what to call the Figure 1. Fasciation (flattened growth) of a pumpkin symptoms caused by R. fascians. Shoot stem, which may be due to disease, a genetic proliferation and leafy galls are sometimes condition, or injury. called “fasciation,” a term also used to refer to tissues that grow into a flattened ribbon- like manner (Figure 1). The root for the word fasciation come from the Latin, fascia, to fuse, and refers to a joining of tissues. We will reserve the term fasciation for the ribbon like growth of stems and other organs. The terms “leafy gall” and “shoot proliferation” are unfamiliar to many people, but are a good description of what is seen on affected plants. A leafy gall is a mass of buds or short shoots tightly packed together and fused at the base. These may appear beneath the soil or near the soil line at the base of the stem (Figure 2). -
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. -
Calameuta Konow 1896 Trachelastatus Morice and Durrant 1915 Syn
105 NOMINA INSECTA NEARCTICA Calameuta Konow 1896 Trachelastatus Morice and Durrant 1915 Syn. Monoplopus Konow 1896 Syn. Neateuchopus Benson 1935 Syn. Haplocephus Benson 1935 Syn. Microcephus Benson 1935 Syn. Calameuta clavata Norton 1869 (Phylloecus) Trachelus tabidus Fabricius 1775 (Sirex) Sirex macilentus Fabricius 1793 Syn. Cephus Latreille 1802 Cephus mandibularis Lepeletier 1823 Syn. Astatus Jurine 1801 Unav. Cephus nigritus Lepeletier 1823 Syn. Perinistilus Ghigi 1904 Syn. Cephus vittatus Costa 1878 Syn. Peronistilomorphus Pic 1916 Syn. Calamenta [sic] johnsoni Ashmead 1900 Syn. Fossulocephus Pic 1917 Syn. Pseudocephus Dovnar-Zapolskii 1931 Syn. Cephus cinctus Norton 1872 (Cephus) CERAPHRONIDAE Cephus occidentalis Riley and Marlatt 1891 Syn. Cephus graenicheri Ashmead 1898 Syn. Cephus pygmaeus Linnaeus 1766 (Sirex) Tenthredo longicornis Geoffroy 1785 Syn. Aphanogmus Thomson 1858 Tenthredo polygona Gmelin 1790 Syn. Banchus spinipes Panzer 1801 Syn. Aphanogmus bicolor Ashmead 1893 (Aphanogmus) Astatus floralis Klug 1803 Syn. Aphanogmus claviger Kieffer 1907 Syn. Banchus viridator Fabricius 1804 Syn. Ceraphron reitteri Kieffer 1907 Syn. Cephus subcylindricus Gravenhorst 1807 Syn. Aphanogmus canadensis Whittaker 1930 (Aphanogmus) Cephus leskii Lepeletier 1823 Syn. Aphanogmus dorsalis Whittaker 1930 (Aphanogmus) Cephus atripes Stephens 1835 Syn. Aphanogmus floridanus Ashmead 1893 (Aphanogmus) Cephus flavisternus Costa 1882 Syn. Aphanogmus fulmeki Szelenyi 1940 (Aphanogmus) Cephus clypealis Costa 1894 Syn. Aphanogmus parvulus Roberti 1954 Syn. Cephus notatus Kokujev 1910 Syn. Aphanogmus fumipennis Thomson 1858 (Aphanogmus) Cephus tanaiticus Dovnar-Zapolskii 1926 Syn. Aphanogmus grenadensis Ashmead 1896 Syn. Aphanogmus formicarius Kieffer 1905 Syn. Hartigia Schiodte 1838 Ceraphron formicarum Kieffer 1907 Syn. Cerobractus Costa 1860 Syn. Aphanogmus clavatus Kieffer 1907 Syn. Macrocephus Schlechtendal 1878 Syn. Cerphron armatus Kieffer 1907 Syn. Cephosoma Gradl 1881 Syn. -
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 ................................................................................................. -
Butlleti 71.P65
Butll. Inst. Cat. Hist. Nat., 71: 83-95. 2003 ISSN: 1133-6889 GEA, FLORA ET FAUNA The life cycle of Andricus hispanicus (Hartig, 1856) n. stat., a sibling species of A. kollari (Hartig, 1843) (Hymenoptera: Cynipidae) Juli Pujade-Villar*, Roger Folliot** & David Bellido* Rebut: 28.07.03 Acceptat: 01.12.03 Abstract and so we consider A. mayeti and A. niger to be junior synonyms of A. hispanicus. Finally, possible causes of the speciation of A. kollari and The marble gallwasp, Andricus kollari, common A. hispanicus are discussed. and widespread in the Western Palaeartic, is known for the conspicuous globular galls caused by the asexual generations on the buds of several KEY WORDS: Cynipidae, Andricus, A. kollari, A. oak species. The sexual form known hitherto, hispanicus, biological cycle, sibling species, formerly named Andricus circulans, makes small sexual form, speciation, distribution, morphology, gregarious galls on the buds of Turkey oak, A. mayeti, A. burgundus. Quercus cerris; this oak, however, is absent from the Iberian Peninsula, where on the other hand the cork oak, Q. suber, is present. Recent genetic studies show the presence of two different Resum populations or races with distribution patterns si- milar to those of Q. cerris and Q. suber. We present new biological and morphological Cicle biològic d’Andricus hispanicus (Hartig, evidence supporting the presence of a sibling 1856) una espècie bessona d’A. kollari (Hartig, species of A. kollari in the western part of its 1843) (Hymenoptera: Cynipidae) range (the Iberian Peninsula, southern France and North Africa), Andricus hispanicus n. stat.. Biological and morphological differences separating these Andricus kollari és una espècie molt comuna dis- two species from other closely related ones are tribuida a l’oest del paleartic coneguda per la given and the new sexual form is described for the gal·la globular i relativament gran de la generació first time. -
Hawai'i Landscape Plant Pest Guide: Mites and Gall-Forming Insects
Insect Pests February 2015 IP-35 Hawai‘i Landscape Plant Pest Guide: Mites And Gall-Forming Insects Arnold Hara & Ruth Niino-DuPonte Department of Plant & Environmental Protection Sciences Coconut Mite (Aceria guerreronis) Identification and Damage • Mites are microscopic and translucent, and may appear only as a silvery patch when viewed with a 10x hand lens. • Coconut mite populations peak about half way through the 12-month-long development of coconut fruit, and decline so that very few, if any, mites remain on mature coconuts. • Coconut mites disperse by wind or by being carried on insects or birds. Perianth of coconut In dense plantings, mites may be able to crawl between plants. • Mites pierce tender tissue under the perianth protecting the stem end of immature coconut fruit. As fruit matures, the damaged tissue emerges as a pale patch from the perianth. When exposed to air, the tissue develops a cork-like surface with deep cracks. • Fruits may prematurely drop or be deformed, stunted, and scarred. • The coconut mite appears to only affect coconut palms; coconut palm varieties and related species may differ in their susceptibility to this mite. Corky tissue emerges from perianth What to Do • Prune all coconuts in all stages of development to eliminate coconut mite populations. • Predatory mites and some fungi (especially under humid conditions) attack the coconut mite but may not be sufficient to control heavy infestations. • Select coconut palm varieties that are less susceptible to coconut mites. • Contact miticides need to be applied frequently and continuously to provide control. Miticides must be EPA registered for use on coconut for Closeup of corky damage human consumption of edible coconut flesh. -
The Chestnut Blight Fungus for Studies on Virus/Host and Virus/Virus Interactions: from a Natural to a Model Host
Virology 477 (2015) 164–175 Contents lists available at ScienceDirect Virology journal homepage: www.elsevier.com/locate/yviro The chestnut blight fungus for studies on virus/host and virus/virus interactions: From a natural to a model host Ana Eusebio-Cope a, Liying Sun b, Toru Tanaka a, Sotaro Chiba a, Shin Kasahara c, Nobuhiro Suzuki a,n a Institute of Plant Science and Resources (IPSR), Okayama University, Chuou 2-20-1, Kurashiki, Okayama 710-0046, Japan b College of Plant Protection, Northwest A & F University, Yangling, Shananxi, China c Department of Environmental Sciences, Miyagi University, Sendai 982-215, Japan article info abstract Article history: The chestnut blight fungus, Cryphonectria parasitica, is an important plant pathogenic ascomycete. The Received 16 August 2014 fungus hosts a wide range of viruses and now has been established as a model filamentous fungus for Returned to author for revisions studying virus/host and virus/virus interactions. This is based on the development of methods for 15 September 2014 artificial virus introduction and elimination, host genome manipulability, available host genome Accepted 26 September 2014 sequence with annotations, host mutant strains, and molecular tools. Molecular tools include sub- Available online 4 November 2014 cellular distribution markers, gene expression reporters, and vectors with regulatable promoters that Keywords: have been long available for unicellular organisms, cultured cells, individuals of animals and plants, and Cryphonectria parasitica certain filamentous fungi. A comparison with other filamentous fungi such as Neurospora crassa has been Chestnut blight fungus made to establish clear advantages and disadvantages of C. parasitica as a virus host. In addition, a few dsRNA recent studies on RNA silencing vs. -
NDP 11 V2 - National Diagnostic Protocol for Cryphonectria Parasitica
NDP 11 V2 - National Diagnostic Protocol for Cryphonectria parasitica National Diagnostic Protocol Chestnut blight Caused by Cryphonectria parasitica NDP 11 V2 NDP 11 V2 - National Diagnostic Protocol for Cryphonectria parasitica © Commonwealth of Australia Ownership of intellectual property rights Unless otherwise noted, copyright (and any other intellectual property rights, if any) in this publication is owned by the Commonwealth of Australia (referred to as the Commonwealth). Creative Commons licence All material in this publication is licensed under a Creative Commons Attribution 3.0 Australia Licence, save for content supplied by third parties, logos and the Commonwealth Coat of Arms. Creative Commons Attribution 3.0 Australia Licence is a standard form licence agreement that allows you to copy, distribute, transmit and adapt this publication provided you attribute the work. A summary of the licence terms is available from http://creativecommons.org/licenses/by/3.0/au/deed.en. The full licence terms are available from https://creativecommons.org/licenses/by/3.0/au/legalcode. This publication (and any material sourced from it) should be attributed as: Subcommittee on Plant Health Diagnostics (2017). National Diagnostic Protocol for Cryphonectria parasitica – NDP11 V2. (Eds. Subcommittee on Plant Health Diagnostics) Authors Cunnington, J, Mohammed, C and Glen, M. Reviewers Pascoe, I and Tan YP, ISBN 978-0- 9945113-6-2. CC BY 3.0. Cataloguing data Subcommittee on Plant Health Diagnostics (2017). National Diagnostic Protocol for Cryphonectria parasitica – NDP11 V2. (Eds. Subcommittee on Plant Health Diagnostics) Authors Cunnington, J, Mohammed, C and Glen, M. Reviewers Pascoe, I and Tan YP, ISBN 978-0-9945113-6-2. -
Restoration of the American Chestnut in New Jersey
U.S. Fish & Wildlife Service Restoration of the American Chestnut in New Jersey The American chestnut (Castanea dentata) is a tree native to New Jersey that once grew from Maine to Mississippi and as far west as Indiana and Tennessee. This tree with wide-spreading branches and a deep broad-rounded crown can live 500-800 years and reach a height of 100 feet and a diameter of more than 10 feet. Once estimated at 4 billion trees, the American chestnut Harvested chestnuts, early 1900's. has almost been extirpated in the last 100 years. The U.S. Fish and Wildlife Service, New Jersey Field Value Office (Service) and its partners, including American Chestnut The American chestnut is valued Cooperators’ Foundation, American for its fruit and lumber. Chestnuts Chestnut Foundation, Monmouth are referred to as the “bread County Parks, Bayside State tree” because their nuts are Prison, Natural Lands Trust, and so high in starch that they can several volunteers, are working to American chestnut leaf (4"-8"). be milled into flour. Chestnuts recover the American chestnut in can be roasted, boiled, dried, or New Jersey. History candied. The nuts that fell to the ground were an important cash Chestnuts have a long history of crop for families in the northeast cultivation and use. The European U.S. and southern Appalachians chestnut (Castanea sativa) formed up until the twentieth century. the basis of a vital economy in Chestnuts were taken into towns the Mediterranean Basin during by wagonload and then shipped Roman times. More recently, by train to major markets in New areas in Southern Europe (such as York, Boston, and Philadelphia. -
The Beat Sheet
Subscribe Past Issues Translate RSS View this email in your browser The Beat Sheet Newsletter of the Frost Entomological Museum Fall 2020 Note: Our public museum is still closed due to COVID-19 safety precautions and Penn State regulations. We will let you know when we receive more information. Thank you for your patience! New Species Discovery? Oak gall wasps (Cynipoidea) have been the dominant research interest of Frost personnel over the past few months. Through regular monitoring of local oak populations, we've found some truly striking galls and made surprising observations along the way. Most exciting, perhaps, is that there seem to be 3 gall inquilines that have been reared from Philonix nigra and Callirhytis favosa galls that do not key to any known species nor do they match any known species descriptions. Perhaps they are new to science! We still need to verify this result with a comprehensive look at their morphology and by sequencing their DNA, but the project already is yielding exciting discoveries. Above: Gall created by Philonix nigra (left) and Callirhytis favosa (right) that unknown inquilines were reared from. Guide to the Gall Wasps of the Eastern US — Coming soon! Museum Director Andy Deans has taken sabbatical this fall to devote time and energy into developing a resource that will serve as a guide to oak galls wasps of the Eastern US. The current sources, mainly books by Ephraim Felt (1940) and Weld (1959), need a lot of updating and a better, more field guide-like layout. He’s compiling species’s natural history data, including seasonal phenology, host use, gall characteristics, and differences in biology and behavior of the alternating generations where they occur. -
UNIVERSITY of WISCONSIN-LA CROSSE Graduate Studies
UNIVERSITY OF WISCONSIN-LA CROSSE Graduate Studies BIOLOGICAL CONTROL OF CRYPHONECTRIA PARASITICA WITH STREPTOMYCES AND AN ANALYSIS OF VEGETATIVE COMPATIBILITY DIVERSITY OF CRYPHONECTRIA PARASITICA IN WISCONSIN, USA. A Manuscript Style Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biology Ashley R. Smith College of Science and Allied Health Biology December, 2013 ABSTRACT Smith, A.S. Biological control of Cryphonectria parasitica with Streptomyces and an analysis of vegetative compatibility diversity of Cryphonectria parasitica in Wisconsin, USA. MS in Biology, December 2013, 52pp. (A. Baines) The American chestnut tree (Castanea dentata) has been plagued by the fungal pathogen Cryphonectria parasitica. While the primary biological control treatment has relied upon the use of hypovirus, a mycovirus that reduces the virulence of C. parasitica, here the potential for a Streptomyces inoculum as a biological control is explored. Two Wisconsin stands of infected chestnut in Galesville and Rockland were inoculated with hypovirus and Streptomyces using a randomized block design. At these stands the Streptomyces treatment reduced canker length expansion rates more than the hypovirus treatments and control. The Streptomyces treatment had significantly lower canker width expansion rates compared to the control. In addition to having reduced canker expansion rates, the trees inoculated with Streptomyces had the lowest mortality rate. The diversity of the fungus was low at the study sites and consisted of only two known vegetative compatibility types at each stand. This low level of diversity made it ideal for hypovirus dispersal, and for limiting canker expansion rates. This research supports the hypothesis that Streptomyces treatment is an effective alternative to hypovirus treatment that may prove beneficial in areas where hypovirus efforts have failed.