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ARTHROPOD COMMUNITIES and PASSERINE DIET: EFFECTS of SHRUB EXPANSION in WESTERN ALASKA by Molly Tankersley Mcdermott, B.A./B.S
Arthropod communities and passerine diet: effects of shrub expansion in Western Alaska Item Type Thesis Authors McDermott, Molly Tankersley Download date 26/09/2021 06:13:39 Link to Item http://hdl.handle.net/11122/7893 ARTHROPOD COMMUNITIES AND PASSERINE DIET: EFFECTS OF SHRUB EXPANSION IN WESTERN ALASKA By Molly Tankersley McDermott, B.A./B.S. A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biological Sciences University of Alaska Fairbanks August 2017 APPROVED: Pat Doak, Committee Chair Greg Breed, Committee Member Colleen Handel, Committee Member Christa Mulder, Committee Member Kris Hundertmark, Chair Department o f Biology and Wildlife Paul Layer, Dean College o f Natural Science and Mathematics Michael Castellini, Dean of the Graduate School ABSTRACT Across the Arctic, taller woody shrubs, particularly willow (Salix spp.), birch (Betula spp.), and alder (Alnus spp.), have been expanding rapidly onto tundra. Changes in vegetation structure can alter the physical habitat structure, thermal environment, and food available to arthropods, which play an important role in the structure and functioning of Arctic ecosystems. Not only do they provide key ecosystem services such as pollination and nutrient cycling, they are an essential food source for migratory birds. In this study I examined the relationships between the abundance, diversity, and community composition of arthropods and the height and cover of several shrub species across a tundra-shrub gradient in northwestern Alaska. To characterize nestling diet of common passerines that occupy this gradient, I used next-generation sequencing of fecal matter. Willow cover was strongly and consistently associated with abundance and biomass of arthropods and significant shifts in arthropod community composition and diversity. -
The Ecology, Behavior, and Biological Control Potential of Hymenopteran Parasitoids of Woodwasps (Hymenoptera: Siricidae) in North America
REVIEW:BIOLOGICAL CONTROL-PARASITOIDS &PREDATORS The Ecology, Behavior, and Biological Control Potential of Hymenopteran Parasitoids of Woodwasps (Hymenoptera: Siricidae) in North America 1 DAVID R. COYLE AND KAMAL J. K. GANDHI Daniel B. Warnell School of Forestry and Natural Resources, University of Georgia, Athens, GA 30602 Environ. Entomol. 41(4): 731Ð749 (2012); DOI: http://dx.doi.org/10.1603/EN11280 ABSTRACT Native and exotic siricid wasps (Hymenoptera: Siricidae) can be ecologically and/or economically important woodboring insects in forests worldwide. In particular, Sirex noctilio (F.), a Eurasian species that recently has been introduced to North America, has caused pine tree (Pinus spp.) mortality in its non-native range in the southern hemisphere. Native siricid wasps are known to have a rich complex of hymenopteran parasitoids that may provide some biological control pressure on S. noctilio as it continues to expand its range in North America. We reviewed ecological information about the hymenopteran parasitoids of siricids in North America north of Mexico, including their distribution, life cycle, seasonal phenology, and impacts on native siricid hosts with some potential efÞcacy as biological control agents for S. noctilio. Literature review indicated that in the hymenop- teran families Stephanidae, Ibaliidae, and Ichneumonidae, there are Þve genera and 26 species and subspecies of native parasitoids documented from 16 native siricids reported from 110 tree host species. Among parasitoids that attack the siricid subfamily Siricinae, Ibalia leucospoides ensiger (Norton), Rhyssa persuasoria (L.), and Megarhyssa nortoni (Cresson) were associated with the greatest number of siricid and tree species. These three species, along with R. lineolata (Kirby), are the most widely distributed Siricinae parasitoid species in the eastern and western forests of North America. -
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. -
4 Reproductive Biology of Cerambycids
4 Reproductive Biology of Cerambycids Lawrence M. Hanks University of Illinois at Urbana-Champaign Urbana, Illinois Qiao Wang Massey University Palmerston North, New Zealand CONTENTS 4.1 Introduction .................................................................................................................................. 133 4.2 Phenology of Adults ..................................................................................................................... 134 4.3 Diet of Adults ............................................................................................................................... 138 4.4 Location of Host Plants and Mates .............................................................................................. 138 4.5 Recognition of Mates ................................................................................................................... 140 4.6 Copulation .................................................................................................................................... 141 4.7 Larval Host Plants, Oviposition Behavior, and Larval Development .......................................... 142 4.8 Mating Strategy ............................................................................................................................ 144 4.9 Conclusion .................................................................................................................................... 148 Acknowledgments ................................................................................................................................. -
1 Etiology, Epidemiology and Management of Fruit Rot Of
Etiology, Epidemiology and Management of Fruit Rot of Deciduous Holly in U.S. Nursery Production Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Shan Lin Graduate Program in Plant Pathology The Ohio State University 2018 Dissertation Committee Dr. Francesca Peduto Hand, Advisor Dr. Anne E. Dorrance Dr. Laurence V. Madden Dr. Sally A. Miller 1 Copyrighted by Shan Lin 2018 2 Abstract Cut branches of deciduous holly (Ilex spp.) carrying shiny and colorful fruit are popularly used for holiday decorations in the United States. Since 2012, an emerging disease causing the fruit to rot was observed across Midwestern and Eastern U.S. nurseries. A variety of other symptoms were associated with the disease, including undersized, shriveled, and dull fruit, as well as leaf spots and early plant defoliation. The disease causal agents were identified by laboratory processing of symptomatic fruit collected from nine locations across four states over five years by means of morphological characterization, multi-locus phylogenetic analyses and pathogenicity assays. Alternaria alternata and a newly described species, Diaporthe ilicicola sp. nov., were identified as the primary pathogens associated with the disease, and A. arborescens, Colletotrichum fioriniae, C. nymphaeae, Epicoccum nigrum and species in the D. eres species complex were identified as minor pathogens in this disease complex. To determine the sources of pathogen inoculum in holly fields, and the growth stages of host susceptibility to fungal infections, we monitored the presence of these pathogens in different plant tissues (i.e., dormant twigs, mummified fruit, leaves and fruit), and we studied inoculum dynamics and assessed disease progression throughout the growing season in three Ohio nurseries exposed to natural inoculum over two consecutive years. -
EPPO Reporting Service
ORGANISATION EUROPEENNE EUROPEAN AND MEDITERRANEAN ET MEDITERRANEENNE PLANT PROTECTION POUR LA PROTECTION DES PLANTES ORGANIZATION EPPO Reporting Service NO. 1 PARIS, 2021-01 General 2021/001 New data on quarantine pests and pests of the EPPO Alert List 2021/002 Update on the situation of quarantine pests in the Russian Federation 2021/003 Update on the situation of quarantine pests in Tajikistan 2021/004 Update on the situation of quarantine pests in Uzbekistan 2021/005 New and revised dynamic EPPO datasheets are available in the EPPO Global Database Pests 2021/006 Anoplophora glabripennis eradicated from Austria 2021/007 Popillia japonica is absent from Germany 2021/008 First report of Scirtothrips aurantii in Spain 2021/009 Agrilus planipennis found in Saint Petersburg, Russia 2021/010 First report of Spodoptera frugiperda in Syria 2021/011 Spodoptera frugiperda found in New South Wales, Australia 2021/012 Spodoptera ornithogalli (Lepidoptera Noctuidae - yellow-striped armyworm): addition to the EPPO Alert List 2021/013 First report of Xylosandrus compactus in mainland Spain 2021/014 First report of Eotetranychus lewisi in mainland Portugal 2021/015 First report of Meloidogyne chitwoodi in Spain 2021/016 Update on the situation of the potato cyst nematodes Globodera rostochiensis and G. pallida in Portugal Diseases 2021/017 First report of tomato brown rugose fruit virus in Belgium 2021/018 Update on the situation of tomato brown rugose fruit virus in Spain 2021/019 Update on the situation of Acidovorax citrulli in Greece with findings -
Identification Key to the Subfamilies of Ichneumonidae (Hymenoptera)
Identification key to the subfamilies of Ichneumonidae (Hymenoptera) Gavin Broad Dept. of Entomology, The Natural History Museum, Cromwell Road, London SW7 5BD, UK Notes on the key, February 2011 This key to ichneumonid subfamilies should be regarded as a test version and feedback will be much appreciated (emails to [email protected]). Many of the illustrations are provisional and more characters need to be illustrated, which is a work in progress. Many of the scanning electron micrographs were taken by Sondra Ward for Ian Gauld’s series of volumes on the Ichneumonidae of Costa Rica. Many of the line drawings are by Mike Fitton. I am grateful to Pelle Magnusson for the photographs of Brachycyrtus ornatus and for his suggestion as to where to include this subfamily in the key. Other illustrations are my own work. Morphological terminology mostly follows Fitton et al. (1988). A comprehensively illustrated list of morphological terms employed here is in development. In lateral views, the anterior (head) end of the wasp is to the left and in dorsal or ventral images, the anterior (head) end is uppermost. There are a few exceptions (indicated in figure legends) and these will rectified soon. Identifying ichneumonids Identifying ichneumonids can be a daunting process, with about 2,400 species in Britain and Ireland. These are currently classified into 32 subfamilies (there are a few more extralimitally). Rather few of these subfamilies are reconisable on the basis of simple morphological character states, rather, they tend to be reconisable on combinations of characters that occur convergently and in different permutations across various groups of ichneumonids. -
Proceedings, 23Rd U.S. Department of Agriculture Interagency Research
United States Department of Proceedings Agriculture 23rd U.S. Department of Agriculture Forest Service Northern Interagency Research Forum on Research Station Invasive Species 2012 General Technical Report NRS-P-114 The findings and conclusions of each article in this publication are those of the individual author(s) and do not necessarily represent the views of the U.S. Department of Agriculture or the Forest Service. All articles were received in digital format and were edited for uniform type and style. Each author is responsible for the accuracy and content of his or her paper. The use of trade, firm, or corporation names in this publication is for the information and convenience of the reader. Such use does not constitute an official endorsement or approval by the U.S. Department of Agriculture or the Forest Service of any product or service to the exclusion of others that may be suitable. 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 fi sh or other wildlife—if they are not handled or applied properly. Use all pesticides selectively and carefully. Follow recommended practices for the disposal of surplus pesticides and pesticide containers. Cover graphic by Vincent D’Amico, U.S. Forest Service, Northern Research Station. Manuscript received for publication August 2012 Published by: For additional copies: U.S. -
Patterns of Woodboring Beetle Activity Following Fires and Bark Beetle Outbreaks in Montane Forests of California, USA Chris Ray1* , Daniel R
Ray et al. Fire Ecology (2019) 15:21 Fire Ecology https://doi.org/10.1186/s42408-019-0040-1 ORIGINAL RESEARCH Open Access Patterns of woodboring beetle activity following fires and bark beetle outbreaks in montane forests of California, USA Chris Ray1* , Daniel R. Cluck2, Robert L. Wilkerson1, Rodney B. Siegel1, Angela M. White3, Gina L. Tarbill3, Sarah C. Sawyer4 and Christine A. Howell5 Abstract Background: Increasingly frequent and severe drought in the western United States has contributed to more frequent and severe wildfires, longer fire seasons, and more frequent bark beetle outbreaks that kill large numbers of trees. Climate change is expected to perpetuate these trends, especially in montane ecosystems, calling for improved strategies for managing Western forests and conserving the wildlife that they support. Woodboring beetles (e.g., Buprestidae and Cerambycidae) colonize dead and weakened trees and speed succession of habitats altered by fire or bark beetles, while serving as prey for some early-seral habitat specialists, including several woodpecker species. To understand how these ecologically important beetles respond to different sources of tree mortality, we sampled woodborers in 16 sites affected by wildfire or bark beetle outbreak in the previous one to eight years. Study sites were located in the Sierra Nevada, Modoc Plateau, Warner Mountains, and southern Cascades of California, USA. We used generalized linear mixed models to evaluate hypotheses concerning the response of woodboring beetles to disturbance type, severity, and timing; forest stand composition and structure; and tree characteristics. Results: Woodborer activity was often similar in burned and bark beetle outbreak sites, tempered by localized responses to bark beetle activity, burn severity, tree characteristics, and apparent response to ignition date. -
Sirex Noctilio
O R E ST E ST PE C IE S R O FIL E F P S P November 2007 Sirex noctilio Fabricius, 1793 Other scientific names: Sirex melanocerus Thomson, 1871; Paururus noctilio Order and Family: Hymenoptera: Siricidae Common names: European woodwasp; sirex; sirex woodwasp; steel-blue horntail Sirex noctilio is a major global threat to forests and the forest sector causing considerable damage and costs for control. In 1900, this pest was reported from New Zealand which represented the first time it was recorded outside of its native range. Since then it has gradually spread around the globe – to Australia in the 1960s, Latin America and the Caribbean in the 1980s, Africa in the 1990s and North America in this decade. Adult sirex woodwasps – male (L), female (R) (Photos: David R. Lance, USDA APHIS PPQ, Bugwood.org) DISTRIBUTION Native: Europe, Asia, northern Africa (Algeria, Morocco, Tunisia) Introduced: Africa: South Africa (1994) Asia and the Pacific: Australia (1961), New Zealand (1900), Tasmania (1952) Latin America and the Caribbean: Argentina (1985), Brazil (1988), Chile (2001), Uruguay (1980) North America: Canada (2005), US (2004) IDENTIFICATION Eggs are cylindrical, creamy white and approximately 0.30-0.35 mm wide and 1.35-1.56 mm long (Ciesla, 2003b). Larvae are creamy white in colour, legless with a distinctive dark spine at the posterior end (TPCP, n.d.). Length varies but larvae can reach up to 30 mm in length. Adult wasps are metallic blue-black in colour with two pairs of clear yellow membranous wings, black antennae and an upturned, spear-shaped spine or plate (cornus) at the end of the abdomen (TPCP, n.d.; W alker, 2006). -
EPPO Reporting Service
ORGANISATION EUROPEENNE EUROPEAN AND ET MEDITERRANEENNE MEDITERRANEAN POUR LA PROTECTION DES PLANTES PLANT PROTECTION ORGANIZATION OEPP Service d’Information NO. 8 PARIS, 2017-08 Général 2017/145 Nouvelles données sur les organismes de quarantaine et les organismes nuisibles de la Liste d’Alerte de l’OEPP 2017/146 Liste de quarantaine de l'Union Économique Eurasiatique (EAEU) 2017/147 Kits de communication de l’OEPP : nouveaux modèles d’affiches et de brochures sur les organismes nuisibles Ravageurs 2017/148 Rhynchophorus ferrugineus n’est pas présent en Australie 2017/149 Platynota stultana (Lepidoptera : Tortricidae) : à nouveau ajouté sur la Liste d’Alerte de l’OEPP Maladies 2017/150 Premier signalement de Puccinia hemerocallidis au Portugal 2017/151 Premier signalement de Pantoea stewartii en Malaisie 2017/152 La maladie de la léprose des agrumes est associée à plusieurs virus 2017/153 Brevipalpus phoenicis, vecteur de la léprose des agrumes, est un complexe d'espèces Plantes envahissantes 2017/154 Potentiel suppressif de certaines graminées sur la croissance et le développement d’Ambrosia artemisiifolia 2017/155 Bidens subalternans dans la région OEPP : addition à la Liste d’Alerte de l’OEPP 2017/156 Les contraintes abiotiques et la résistance biotique contrôlent le succès de l’établissement d’Humulus scandens 21 Bld Richard Lenoir Tel: 33 1 45 20 77 94 E-mail: [email protected] 75011 Paris Fax: 33 1 70 76 65 47 Web: www.eppo.int OEPP Service d’Information 2017 no. 8 – Général 2017/145 Nouvelles données sur les organismes de quarantaine et les organismes nuisibles de la Liste d’Alerte de l’OEPP En parcourant la littérature, le Secrétariat de l’OEPP a extrait les nouvelles informations suivantes sur des organismes de quarantaine et des organismes nuisibles de la Liste d’Alerte de l’OEPP (ou précédemment listés). -
Leaf-Inhabiting Genera of the Gnomoniaceae, Diaporthales
Studies in Mycology 62 (2008) Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales M.V. Sogonov, L.A. Castlebury, A.Y. Rossman, L.C. Mejía and J.F. White CBS Fungal Biodiversity Centre, Utrecht, The Netherlands An institute of the Royal Netherlands Academy of Arts and Sciences Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales STUDIE S IN MYCOLOGY 62, 2008 Studies in Mycology The Studies in Mycology is an international journal which publishes systematic monographs of filamentous fungi and yeasts, and in rare occasions the proceedings of special meetings related to all fields of mycology, biotechnology, ecology, molecular biology, pathology and systematics. For instructions for authors see www.cbs.knaw.nl. EXECUTIVE EDITOR Prof. dr Robert A. Samson, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] LAYOUT EDITOR Marianne de Boeij, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] SCIENTIFIC EDITOR S Prof. dr Uwe Braun, Martin-Luther-Universität, Institut für Geobotanik und Botanischer Garten, Herbarium, Neuwerk 21, D-06099 Halle, Germany. E-mail: [email protected] Prof. dr Pedro W. Crous, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] Prof. dr David M. Geiser, Department of Plant Pathology, 121 Buckhout Laboratory, Pennsylvania State University, University Park, PA, U.S.A. 16802. E-mail: [email protected] Dr Lorelei L. Norvell, Pacific Northwest Mycology Service, 6720 NW Skyline Blvd, Portland, OR, U.S.A.