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Season Extenders in the Flower Garden by Pat Holloway and Pat Wagner
University of Alaska Fairbanks School of Natural Resources and Extension Georgeson Botanical Notes No. 57 (1993) - Revised 2014 Season Extenders in the Flower Garden by Pat Holloway and Pat Wagner No one gardening in Alaska needs to be reminded that the growing season is very short, especially after the summer of 1992 when the frost-free season at the Garden extended only from May 16 to September 10, and the snow-free season was the shortest ever recorded. Every year we survey the Garden after our first hard frost to identify flowers that still look good and can provide a bit of color even as the days get shorter and we begin to anticipate the first snowfall. On the following page is a list of annuals and perennials that sur- vived the first severe frost on September 10 with an overnight low of 13°F (-10°C). In some instances, only the foliage survived, but they still provided a bit of green color at season’s end. Prior to September 10, temperatures at or slightly below 32°F (0°C) were recorded on three dates, but damage was negligible. Although the flower beds are located fairly close together on a gently sloping hillside, we noticed some differences in damage in the various beds. Flowers in one bed survived the frost, whereas plants of the same species in an adjacent bed were killed. This may be related to differences in cultivars since we did not repeat cultivars in different beds, but it also could be related to slight differences in microclimate from one bed to another. -
Perennials For
Perennials for Sun Botanic Name Common Name Achillea millefolium “Appleblossom” Appleblossom Yarrow Achillea millefolium “Paprika” Paprika Yarrow Achillea “Moonshine” Moonshine Yarrow Achillea “Summer Wine” Summer Wine Yarrow Achillea “Terracotta” Terracotta Yarrow Agastache aurantiaca “Coronado” Coronado Hyssop Agastache “Blue Fortune” Blue Fortune Hyssop Agastache cana Hummingbird Mint Agastache cana “Sonoran Sunset” Sonoran Sunset Hyssop Agastache “Coronado Red” Coronado Red Hyssop Agastache rupestris “Sunset” Sunset Hyssop Alea rosea Hollyhock Alyssum montanum Mountain Gold Alyssum Amorpha canescens Leadplant Amsonia jonesii Colorado Desert Blue Star Amsonia hubrichtii Blue Star Anacyclus depressus Mat Daisy Anchusa azurea Bugloss Antennaria dioica Pussytoes Anthemis marshalliana Golden Marguerite Anthemis “Sauce Hollandaise” Ox-eye Chamomile Arabis blepharophylla “Spring Charm” Rock Cress Arabis causcasica “Snow cap” White Rock Cress Armeria maritime Thrift, Sea Pinks Artemisia “Powis Castle” Powis Castle Wormwood Artemisia schmidtiana “Silver Mound” Silver Mound Wormwood Artemisia stelleriana “Silver Brocade” Silver Brocade Wormwood Artemisia versicolor “Seafoam” Sea Foam Wormwood Asclepias tuberosa Butterfly Weed Aster alpinus Alpine Aster Aster frikarti Monk’s Aster Aster nova angliae New England Aster Aster nova belgii Michaelmas Aster Aubrieta Purple Rock Cress Aurinia saxatilis Basket of Gold Baptisia australis False Indigo Belamcanda chinensis Blackberry Lily Berlandiera lyrata Chocolate Flower Boltonia asteroids Star Flower -
UNIVERSITÀ DEGLI STUDI DEL MOLISE Department
UNIVERSITÀ DEGLI STUDI DEL MOLISE Department of Agricultural, Environmental and Food Sciences Ph.D. course in: AGRICULTURE TECHNOLOGY AND BIOTECHNOLOGY (CURRICULUM: Sustainable plant production and protection) (CYCLE XXIX) Ph.D. thesis NEW INSIGHTS INTO THE BIOLOGY AND ECOLOGY OF THE INSECT VECTORS OF APPLE PROLIFERATION FOR THE DEVELOPMENT OF SUSTAINABLE CONTROL STRATEGIES Coordinator of the Ph.D. course: Prof. Giuseppe Maiorano Supervisor: Prof. Antonio De Cristofaro Co-Supervisor: Dr. Claudio Ioriatti Ph.D. student: Tiziana Oppedisano Matr: 151603 2015/2016 “Nella vita non c’è nulla da temere, c’è solo da capire.” (M. Curie) Index SUMMARY 5 RIASSUNTO 9 INTRODUCTION 13 Phytoplasmas 13 Taxonomy 13 Morphology 14 Symptomps 15 Transmission and spread 15 Detection 17 Phytoplasma transmission by insect vectors 17 Phytoplasma-vector relationship 18 Homoptera as vectors of phytoplasma 19 ‘Candidatus Phytoplasma mali’ 21 Symptomps 21 Distribution in the tree 22 Host plant 24 Molecular characterization and diagnosis 24 Geographical distribution 25 AP in Italy 25 Transmission of AP 27 Psyllid vectors of ‘Ca. P. mali’ 28 Cacopsylla picta Förster (1848) 29 Cacopsylla melanoneura Förster (1848) 32 Other known vectors 36 Disease control 36 Aims of the research 36 References 37 CHAPTER 1: Apple proliferation in Valsugana: three years of disease and psyllid vectors’ monitoring 49 CHAPTER 2: Evaluation of the current vectoring efficiency of Cacopsylla melanoneura and Cacopsylla picta in Trentino 73 CHAPTER 3: The insect vector Cacopsylla picta vertically -
Biodiversa-Project Description-Final Version-110213
1.A. Detailed description of the research area and research plan Context of the proposal Biological invasions (bioinvasions) are defined as the successful establishment and spread of species outside their native range. They act as a major driver of global changes in species distribution. Diverse organisms and ecosystems may be involved, and although not all invasions have a negative impact, the ecological consequences often include the loss of native biological diversity and changes in community structure and ecosystem activity. There may also be additional negative effects on agriculture, forests, fisheries, and human health. National governments, intergovernmental structures like the European Commission and international organizations such as EPPO, CABI and IUCN have therefore mobilized to (i) introduce international laws on invasive species, (ii) organize international networks of scientists and stakeholders to study bioinvasions, and (iii) formalize the cooperation between national environmental or agricultural protection agencies (e.g. the French Agence Nationale de Sécurité Sanitaire, ANSES). Several billion euros are spent annually to address the problems caused by bioinvasions and the scientific community has focused on predicting and controlling future invasions by understanding how they occur. A peer-reviewed journal entitled "Biological Invasions” has been published since 1999. Ecologists have long drawn attention to the negative ecological effects of invasive species, whereas the evolutionary aspects of bioinvasions have received comparatively little attention. This reflects the fact that: i) invasive populations were thought to experience significant bottlenecks during their introduction to new environments and thus possess a limited potential to evolve; and ii) evolution was considered too slow to play a significant role given the relatively short timescale of the invasion process. -
In Vitro Callus Culture of Dianthus Chinensis L. for Assessment of Flavonoid Related Gene Expression Pro Le
In Vitro Callus Culture of Dianthus Chinensis L. for Assessment of Flavonoid Related Gene Expression Prole R. Sreelekshmi University of Kerala Elenjikkal A Siril ( [email protected] ) University of Kerala https://orcid.org/0000-0002-4956-8428 Research Article Keywords: China pink, In vitro avonoid production, Friable callus, 2,4- D, Chalcone synthase Posted Date: March 17th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-320486/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/27 Abstract Dianthus chinensis L. is an edible, ornamental herb used to prepare the Dianthi Herba, a Chinese traditional rejuvenating medicine. Owing to the rapid proliferation of callus tissues, in vitro production of avonoids has their own specic importance. Callus cultures raised followed by auxin directed biosynthesis of avonoid through related transcript prole were carried out. Murashige and Skoog (MS) medium fortied with 2,4- Dichlorophenoxy acetic acid (2,4- D) or picloram induced formation of friable callus from internode derived cultures of D. chinensis. Culture medium containing 2,4- D (10 µM) produced the highest avonoid content, 4.44 mg quercetin equivalent per gram (QE g− 1) under incubation in continuous dark condition, while maximum dry weight yield (0.38 g/ culture) was obtained from 10 µM 2,4- D under 16 h light / 8 h dark condition (50 µmol m− 2 s− 1 irradiance) at 60 days of incubation. The callus raised in light condition in 10 µM 2,4- D selected to analyze avonoid related gene expression prole viz., chalcone synthase (CHS), chalcone isomerase (CHI), avanone-3-hydroxylase (F3H), and avonol synthase (FLS) at specic time intervals. -
Storage of Rose and Carnation Flowers STABY G.L
n 20. Young. E. 1980. Response ofseedling rootstocks ofpeach lo soil n. Verma. B.P. 1979. Container design for reducing root zone tem perature. Proc. SNA Res. Conf. 24:179-182. temperature. HortSciencc 15(3):294-296. 21 Young. K. and K.R.W. Hammct. 1980. Temperature patterns in 18. Wong. T.L.. R.W. Harris, and R.E. Fisscll. 1971. Influence of exposed black polyethylene plant containers. Agr. Mcterol. 21:165— high soil temperatures on five woody-plant species. J. Amcr. Soc. 172. Hon. Sci. 96:( 1)80-83. Young. R.H. and Peynado. 1967. Freeze injury to 3-ycar-old citrus hybrids and varieties following exposure to controlled freez 19. Woodruff. J.G. and N.C. Woodruff. 1934. Pecan root growth and development. J. Agr. Res. 49:511-530. ing conditions. Proc. Rio Grande Val. Hort. Soc. 21:80-88. J. Amer. Soc. Hort. Sci. 109(2): 193-197. 1984. Storage of Rose and Carnation Flowers STABY G.L. Staby,1 M.S. Cunningham,2 C.L. Holstead,3 J.W. Kelly,4 P.S. Konjoian,5 B.A. Eisenbergi6 and B.S. Dressier7 nii jmui Department of Horticulture, The Ohio State University, Columbus, OH 432W Additional index words. Dianthus caryophyllus, Rosa sp.. low pressure storage, hypobaric. controlled atmosphere, tem perature, silver thiosulfate. preservative tAbstracta^ere Normalconductedrefrigerationusing cut flowers(NR), lowof carnationpressureiDianthus(LP, 10 tocaryophyllus35 mm Hg),L.)andandlowroseoxygen(Rosa sp.).(0.5%Vambles^diedto 8%) storage were storage time, gas partial pressures, vapor barriers, chemical pretreatments, grower source, culttvars and stem "cutUng mthods Low oxygen storage was not beneficial regardless of variables tested. -
PRA Cerataphis Lataniae
CSL Pest Risk Analysis for Cerataphis lataniae CSL copyright, 2005 Pest Risk Analysis for Cerataphis lataniae Boisduval STAGE 1: PRA INITIATION 1. What is the name of the pest? Cerataphis lataniae (Boisduval) Hemiptera Aphididae the Latania aphid Synonyms: Ceratovacuna palmae (Baehr) Aphis palmae (Baehr) Boisduvalia lataniae (Boisduval) Note: In the past C. lataniae has been confused with both C. brasiliensis and C. orchidearum (Howard, 2001). As a result it is not always clear which of the older records for host plants and distribution refer to which species. BAYER CODES: CEATLA 2. What is the reason for the PRA? This PRA was initiated following a second interception of this species. Cerataphis lataniae was first intercepted in the UK in 1999 on a consignment of Archontophoenix alexandra and Brahea drandegai, from South Africa. Since then it has been intercepted twice more; on 30/05/02 on Cocos spp. and then again on 13/06/02 on Cocos nucifera. Both the findings in 2002 were at the same botanic garden and there is some suggestion the Coco plants were supplied by the nursery where the first interception was made in 1999. 3. What is the PRA area? As C. lataniae is present within the EU (Germany, Italy, Spain) (See point 11.) this PRA only considers the UK. STAGE 2: PEST RISK ASSESSMENT 4. Does the pest occur in the PRA area or does it arrive regularly as a natural migrant? No. Although Cerataphis lataniae is included on the British checklist this is likely to be an invalid record as there is no evidence to suggest it is established in the UK (R. -
Regulation of Senescence in Carnation (Dianthus Caryophyllus) by Ethylene MODE of ACTION1
Plant Physiol. (1977) 59, 591-593 Regulation of Senescence in Carnation (Dianthus caryophyllus) by Ethylene MODE OF ACTION1 Received for publication April 9, 1976 and in revised form November 16, 1976 SHIMON MAYAK,2 YOASH VAADIA,3 AND DAVID R. DILLEY Department ofHorticulture, Michigan State University, East Lansing, Michigan 48824 ABSTRACT over-all length, and placed individually in 20-ml vials. Flowers Carnation (Dianthus caryophyllus) flowers were exposed to 2 ^i/l were obtained from a local grower and experiments were begun ethylene and examined at intervals to determine the time course of on the day of harvest. Four flowers in a 10-liter desiccator with a wilting, decrease in water uptake, and increase in ionic leakage in CO2 scrubber (NaOH solution) comprised a treatment. Flowers response to ethylene. A rapid decrease in water uptake was observed were exposed to ethylene at 21AI/I for 0, 3, 6, 9, or 12 hr, after which they were ventilated with ethylene-free air at a rate of 100 about 4 hours after initiating treatment with ethylene. This was followed were of 2 ml/min for the remainder of the experiment. Flowers by wilting (in-rolling petals) about hours later. Carbon dioxide observed at 1-hr intervals to determine the onset of wilting inhibited the decline in water uptake and wilting and this is typical of symptoms as judged by in-rolling of petals. most ethylene-induced responses. Ethylene did not affect closure of Effect of Ethylene on Rate of Water Uptake. Cut flowers stomates. Ethylene enhanced ionic leakage, as measured by efflux of 36CI a in which the from the vacuole. -
Aphids (Hemiptera, Aphididae)
A peer-reviewed open-access journal BioRisk 4(1): 435–474 (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2 435 doi: 10.3897/biorisk.4.57 RESEARCH ARTICLE BioRisk www.pensoftonline.net/biorisk Aphids (Hemiptera, Aphididae) Chapter 9.2 Armelle Cœur d’acier1, Nicolas Pérez Hidalgo2, Olivera Petrović-Obradović3 1 INRA, UMR CBGP (INRA / IRD / Cirad / Montpellier SupAgro), Campus International de Baillarguet, CS 30016, F-34988 Montferrier-sur-Lez, France 2 Universidad de León, Facultad de Ciencias Biológicas y Ambientales, Universidad de León, 24071 – León, Spain 3 University of Belgrade, Faculty of Agriculture, Nemanjina 6, SER-11000, Belgrade, Serbia Corresponding authors: Armelle Cœur d’acier ([email protected]), Nicolas Pérez Hidalgo (nperh@unile- on.es), Olivera Petrović-Obradović ([email protected]) Academic editor: David Roy | Received 1 March 2010 | Accepted 24 May 2010 | Published 6 July 2010 Citation: Cœur d’acier A (2010) Aphids (Hemiptera, Aphididae). Chapter 9.2. In: Roques A et al. (Eds) Alien terrestrial arthropods of Europe. BioRisk 4(1): 435–474. doi: 10.3897/biorisk.4.57 Abstract Our study aimed at providing a comprehensive list of Aphididae alien to Europe. A total of 98 species originating from other continents have established so far in Europe, to which we add 4 cosmopolitan spe- cies of uncertain origin (cryptogenic). Th e 102 alien species of Aphididae established in Europe belong to 12 diff erent subfamilies, fi ve of them contributing by more than 5 species to the alien fauna. Most alien aphids originate from temperate regions of the world. Th ere was no signifi cant variation in the geographic origin of the alien aphids over time. -
Aphids and Their Control on Orchids
APHIDS AND THEIR CONTROL ON ORCHIDS Paul J. Johnson, Ph.D. Insect Research Collection, South Dakota State University, Brookings, SD 57007 Aphids are among the most obnoxious of orchid pests. These insects are global and orchid feeding species are problematic in tropical growing areas as well as in commercial and hobby greenhouses in temperate regions. Rabasse and Wyatt (1985) ranked aphids as one of three most serious greenhouse pests, along with spider mites and whiteflies. These pernicious insects can show themselves on orchids year-around in warm climates, but seem to be mostly autumn and winter problems in temperate regions. Like most other orchid pests the most common routes into plant collections is through either the acquisition of an infested plant or the movement of plants from outdoors to indoors. However, certain reproductive stages of pest species do fly and they will move to orchids from other plants quite readily. Because of their propensity for rapid reproduction any action against aphids should be completed quickly while their populations are still small. An aphid infestation is often detected by an accumulation of pale-tan colored “skins” that fall beneath the developing colony. These “skins” are the shed integument from the growing and molting immature aphids. All of the common pest species of aphid also secrete honeydew, a feeding by-product exuded by the aphid and composed of concentrated plant fluids, and is rich in carbohydrates. This honeydew drips and accumulates beneath the aphid colony. Because of the carbohydrates honeydew is attractive to ants, flies, bees, other insects including beneficial species, and sooty mold. -
Identification of Plant DNA in Adults of the Phytoplasma Vector Cacopsylla
insects Article Identification of Plant DNA in Adults of the Phytoplasma Vector Cacopsylla picta Helps Understanding Its Feeding Behavior Dana Barthel 1,*, Hannes Schuler 2,3 , Jonas Galli 4, Luigimaria Borruso 2 , Jacob Geier 5, Katrin Heer 6 , Daniel Burckhardt 7 and Katrin Janik 1,* 1 Laimburg Research Centre, Laimburg 6, Pfatten (Vadena), IT-39040 Auer (Ora), Italy 2 Faculty of Science and Technology, Free University of Bozen-Bolzano, IT-39100 Bozen (Bolzano), Italy; [email protected] (H.S.); [email protected] (L.B.) 3 Competence Centre Plant Health, Free University of Bozen-Bolzano, IT-39100 Bozen (Bolzano), Italy 4 Department of Forest and Soil Sciences, BOKU, University of Natural Resources and Life Sciences Vienna, A-1190 Vienna, Austria; [email protected] 5 Department of Botany, Leopold-Franzens-Universität Innsbruck, Sternwartestraße 15, A-6020 Innsbruck, Austria; [email protected] 6 Faculty of Biology—Conservation Biology, Philipps Universität Marburg, Karl-von-Frisch-Straße 8, D-35043 Marburg, Germany; [email protected] 7 Naturhistorisches Museum, Augustinergasse 2, CH-4001 Basel, Switzerland; [email protected] * Correspondence: [email protected] (D.B.); [email protected] (K.J.) Received: 10 November 2020; Accepted: 24 November 2020; Published: 26 November 2020 Simple Summary: Cacopsylla picta is an insect vector of apple proliferation phytoplasma, the causative bacterial agent of apple proliferation disease. In this study, we provide an answer to the open question of whether adult Cacopsylla picta feed from other plants than their known host, the apple plant. We collected Cacopsylla picta specimens from apple trees and analyzed the composition of plant DNA ingested by these insects. -
Insect Vectors of Phytoplasmas - R
TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol.VII - Insect Vectors of Phytoplasmas - R. I. Rojas- Martínez INSECT VECTORS OF PHYTOPLASMAS R. I. Rojas-Martínez Department of Plant Pathology, Colegio de Postgraduado- Campus Montecillo, México Keywords: Specificity of phytoplasmas, species diversity, host Contents 1. Introduction 2. Factors involved in the transmission of phytoplasmas by the insect vector 3. Acquisition and transmission of phytoplasmas 4. Families reported to contain species that act as vectors of phytoplasmas 5. Bactericera cockerelli Glossary Bibliography Biographical Sketch Summary The principal means of dissemination of phytoplasmas is by insect vectors. The interactions between phytoplasmas and their insect vectors are, in some cases, very specific, as is suggested by the complex sequence of events that has to take place and the complex form of recognition that this entails between the two species. The commonest vectors, or at least those best known, are members of the order Homoptera of the families Cicadellidae, Cixiidae, Psyllidae, Cercopidae, Delphacidae, Derbidae, Menoplidae and Flatidae. The family with the most known species is, without doubt, the Cicadellidae (15,000 species described, perhaps 25,000 altogether), in which 88 species are known to be able to transmit phytoplasmas. In the majority of cases, the transmission is of a trans-stage form, and only in a few species has transovarial transmission been demonstrated. Thus, two forms of transmission by insects generally are known for phytoplasmas: trans-stage transmission occurs for most phytoplasmas in their interactions with their insect vectors, and transovarial transmission is known for only a few phytoplasmas. UNESCO – EOLSS 1. Introduction The phytoplasmas are non culturable parasitic prokaryotes, the mechanisms of dissemination isSAMPLE mainly by the vector insects.