DEFOLIATORS Insect Sections
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Picea Sitchensis (Bong.) Carr. Sitka Spruce Pinaceae Pine Family A
Picea sitchensis (Bong.) Carr. Sitka Spruce Pinaceae Pine family A. S. Harris Sitka spruce (Picea sitchensis), known also as tideland spruce, coast spruce, and yellow spruce, is the largest of the world’s spruces and is one of the most prominent forest trees in stands along the northwest coast of North America. This coastal species is seldom found far from tidewater, where moist maritime air and summer fogs help to main- tain humid conditions necessary for growth. Throughout most of its range from northern Califor- nia to Alaska, Sitka spruce is associated with western hemlock (Tsuga heterophylla) in dense stands where growth rates are among the highest in North America. It is a valuable commercial timber species for lumber, pulp, and many special uses (15,16). Habitat Native Range Sitka spruce (fig. 1) grows in a narrow strip along the north Pacific coast from latitude 61” N. in south- central Alaska to 39” N. in northern California. The most extensive portion of the range in both width and elevation is in southeast Alaska and northern British Columbia, where the east-west range extends for about 210 km (130 mi) to include a narrow main- land strip and the many islands of the Alexander Archipelago in Alaska and the Queen Charlotte Is- lands in British Columbia (24). North and west of southeast Alaska, along the Gulf of Alaska to Prince William Sound, the range is restricted by steep mountains and Piedmont glaciers edging the sea. Within Prince William Sound, the range again widens to about 105 km (65 mi) to include many offshore islands. -
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]. -
Evidence and Implications of Recent and Projected Climate Change in Alaska’S Forest Ecosystems 1, 2 1 3 4 JANE M
Evidence and implications of recent and projected climate change in Alaska’s forest ecosystems 1, 2 1 3 4 JANE M. WOLKEN, TERESA N. HOLLINGSWORTH, T. SCOTT RUPP, F. STUART CHAPIN, III, SARAH F. TRAINOR, 5 6 7 3 8 TARA M. BARRETT, PATRICK F. SULLIVAN, A. DAVID MCGUIRE, EUGENIE S. EUSKIRCHEN, PAUL E. HENNON, 9 10 11 8 1 ERIK A. BEEVER, JEFF S. CONN, LISA K. CRONE, DAVID V. D ’AMORE, NANCY FRESCO, 8 3 12 11 13 THOMAS A. HANLEY, KNUT KIELLAND, JAMES J. KRUSE, TRISTA PATTERSON, EDWARD A. G. SCHUUR, 14 14 DAVID L. VERBYLA, AND JOHN YARIE 1Scenarios Network for Alaska and Arctic Planning, University of Alaska, 3352 College Road, Fairbanks, Alaska 99709 USA 2United States Department of Agriculture Forest Service, Pacific Northwest Research Station, Boreal Ecology Cooperative Research Unit, P.O. Box 756780, University of Alaska, Fairbanks, Alaska 99775 USA 3Institute of Arctic Biology, University of Alaska, Fairbanks, Alaska 99775 USA 4Alaska Center for Climate Assessment and Policy, University of Alaska, 3352 College Road, Fairbanks, Alaska 99709 USA 5United States Department of Agriculture Forest Service, Pacific Northwest Research Station, Anchorage Forestry Sciences Laboratory, 3301 C Street, Suite 200, Anchorage, Alaska 99503 USA 6Environment and Natural Resources Institute, Department of Biological Sciences, University of Alaska, Anchorage, Alaska 99508 USA 7United States Geological Survey, Alaska Cooperative Fish and Wildlife Research Unit, University of Alaska, Fairbanks, Alaska 99775 USA 8United States Department of Agriculture Forest -
The Green Spruce Aphid in Western Europe
Forestry Commission The Green Spruce Aphid in Western Europe: Ecology, Status, Impacts and Prospects for Management Edited by Keith R. Day, Gudmundur Halldorsson, Susanne Harding and Nigel A. Straw Forestry Commission ARCHIVE Technical Paper & f FORESTRY COMMISSION TECHNICAL PAPER 24 The Green Spruce Aphid in Western Europe: Ecology, Status, Impacts and Prospects for Management A research initiative undertaken through European Community Concerted Action AIR3-CT94-1883 with the co-operation of European Communities Directorate-General XII Science Research and Development (Agro-Industrial Research) Edited by Keith R. t)ay‘, Gudmundur Halldorssorr, Susanne Harding3 and Nigel A. Straw4 ' University of Ulster, School of Environmental Studies, Coleraine BT52 ISA, Northern Ireland, U.K. 2 2 Iceland Forest Research Station, Mogilsa, 270 Mossfellsbaer, Iceland 3 Royal Veterinary and Agricultural University, Department of Ecology and Molecular Biology, Thorvaldsenvej 40, Copenhagen, 1871 Frederiksberg C., Denmark 4 Forest Research, Alice Holt Lodge, Wrecclesham, Farnham, Surrey GU10 4LH, U.K. KVL & Iceland forestry m research station Forest Research FORESTRY COMMISSION, EDINBURGH © Crown copyright 1998 First published 1998 ISBN 0 85538 354 2 FDC 145.7:453:(4) KEYWORDS: Biological control, Elatobium , Entomology, Forestry, Forest Management, Insect pests, Picea, Population dynamics, Spruce, Tree breeding Enquiries relating to this publication should be addressed to: The Research Communications Officer Forest Research Alice Holt Lodge Wrecclesham, Farnham Surrey GU10 4LH Front Cover: The green spruce aphid Elatobium abietinum. (Photo: G. Halldorsson) Back Cover: Distribution of the green spruce aphid. CONTENTS Page List of contributors IV Preface 1. Origins and background to the green spruce aphid C. I. Carter and G. Hallddrsson in Europe 2. -
Alder Canopy Dieback and Damage in Western Oregon Riparian Ecosystems
Alder Canopy Dieback and Damage in Western Oregon Riparian Ecosystems Sims, L., Goheen, E., Kanaskie, A., & Hansen, E. (2015). Alder canopy dieback and damage in western Oregon riparian ecosystems. Northwest Science, 89(1), 34-46. doi:10.3955/046.089.0103 10.3955/046.089.0103 Northwest Scientific Association Version of Record http://cdss.library.oregonstate.edu/sa-termsofuse Laura Sims,1, 2 Department of Botany and Plant Pathology, Oregon State University, 1085 Cordley Hall, Corvallis, Oregon 97331 Ellen Goheen, USDA Forest Service, J. Herbert Stone Nursery, Central Point, Oregon 97502 Alan Kanaskie, Oregon Department of Forestry, 2600 State Street, Salem, Oregon 97310 and Everett Hansen, Department of Botany and Plant Pathology, 1085 Cordley Hall, Oregon State University, Corvallis, Oregon 97331 Alder Canopy Dieback and Damage in Western Oregon Riparian Ecosystems Abstract We gathered baseline data to assess alder tree damage in western Oregon riparian ecosystems. We sought to determine if Phytophthora-type cankers found in Europe or the pathogen Phytophthora alni subsp. alni, which represent a major threat to alder forests in the Pacific Northwest, were present in the study area. Damage was evaluated in 88 transects; information was recorded on damage type (pathogen, insect or wound) and damage location. We evaluated 1445 red alder (Alnus rubra), 682 white alder (Alnus rhombifolia) and 181 thinleaf alder (Alnus incana spp. tenuifolia) trees. We tested the correlation between canopy dieback and canker symptoms because canopy dieback is an important symptom of Phytophthora disease of alder in Europe. We calculated the odds that alder canopy dieback was associated with Phytophthora-type cankers or other biotic cankers. -
Integrating Cultural Tactics Into the Management of Bark Beetle and Reforestation Pests1
DA United States US Department of Proceedings --z:;;-;;; Agriculture Forest Service Integrating Cultural Tactics into Northeastern Forest Experiment Station the Management of Bark Beetle General Technical Report NE-236 and Reforestation Pests Edited by: Forest Health Technology Enterprise Team J.C. Gregoire A.M. Liebhold F.M. Stephen K.R. Day S.M.Salom Vallombrosa, Italy September 1-3, 1996 Most of the papers in this publication were submitted electronically and were edited to achieve a uniform format and type face. Each contributor is responsible for the accuracy and content of his or her own paper. Statements of the contributors from outside the U.S. Department of Agriculture may not necessarily reflect the policy of the Department. Some participants did not submit papers so they have not been included. 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. Remarks about pesticides appear in some technical papers contained in these proceedings. Publication of these statements does not constitute endorsement or recommendation of them by the conference sponsors, nor does it imply that uses discussed have been registered. Use of most pesticides is regulated by State and Federal Law. Applicable regulations must be obtained from the appropriate regulatory agencies. CAUTION: Pesticides can be injurious to humans, domestic animals, desirable plants, and fish and other wildlife - if they are not handled and applied properly. -
Bees, Wasps & Ants
Sheringham and Beeston Regis Commons SSSI / SAC FAUNA: Hymenoptera INSECTA (Pterygota) Family/Order English Name. Scientific Name. Authority. Grid Ref. Tetrad/ Last Km sq. Common. Record. HYMENOPTERA. PAMPHILIDAE: Sawfly. Pamphilius inanitus (Villers, 1789) TG1642 1987? (Bees, Wasps and Ants) ARGIDAE: Elm Zig-zag Sawfly. Aproceros leucopoda Takeuchi, 1939 TG1642 14R/B 2020 Bramble Sawfly. Arge cyaneocrocea (Forster, 1771) TG1642 2016 Sawfly. Arge gracilicornis (Klug, 1814 ) TG1642 1987? CIMBICIDAE: Honeysuckle Sawfly. Abia lonicerae (Linnaeus) TG1641 14Q/B 2015 Club-horned Sawfly. Abia sericera (Linnaeus) TG1642 14R/B 2014 Club-horned Sawfly. Zaraea fasciata Linnaeus, 1758 TG1641/42 14R,14Q/B 2014 Birch Sawfly. Cimbex femoratus (Linnaeus, 1758) TG1642 14R/B 2017 SIRICIDAE: Greater Horntail Wasp. Urocerus gigas (Linnaeus, 1758) TG1642 14R/S 1992 CEPHIDAE: Sawfly. Calameuta pallipes (Klug, 1803) TG1642 1987? TENTHREDINIDAE: Willow Sawfly. Pontania proxima (Lepeletier, 1823) TG1642 14R/BS 2009 Willow Sawfly. Eupontania pedunculi (Hartig, 1837) TG1642 14R/B 1999 Willow Sawfly. Eupontainia viminalis (Linnaeus, 1758) TG1642 14R/B 2002 Willow Sawfly. Pontainia bridgemanii (Cameron, 1883) TG1642 14R/B 1999 Sawfly. Caliroa annulipes (Klug, 1816) TG1642 14R/S 2002 Hazel Sawfly. Craesus septentrionalis (Linnaeus, 1758) TG1641 14Q/B 2017 Sawfly. Blennocampa phyllocolpa Viitasaari & Vikberg, 1985 TG1642/41 14R,14Q/B 2003 Sawfly. Selandria serva (Fabricius, 1793) TG1642 14R/B 2013 Sawfly. Aneugmenus padi (Linnaeus, 1761) TG1642 1987? Bracken Sawfly. Strongylogaster multifasciata (Geoffroy, 1785) TG1642 14R/BS 2020 Sawfly. Dichrodolerus vestigialis (Klug, 1818) TG1642 1996 Sawfly. Dolerus germanicus (Fabricius, 1775) TG1642 1987? Sawfly. Eutomostethus ephippium (Panzer, 1798) TG1642 14R/BS 2020 Sawfly. Poodolerus aeneus Hartig, 1837 TG1642 1987? Sawfly. Dolerus brevitarus Hartig TG1642 1987? Sawfly. -
Arthropod Community Structure in Regenerating Douglas-Fir and Red Alder Forests: Influences of Geography, Tree Diversity and Density
AN ABSTRACT OF THE THESIS OF Brett L. Schaerer for the degree of Master of Science in Entomology presentedon March 17, 2000. Title: Arthropod Community Structure in Regenerating Douglas-fir and Red Alder Forests: Influences of Geography, Tree Diversity and Density Abstract approved: Redacted for privacy Timothy D. Schowalter The structuring of canopy arthropod communities was reviewed and investigated in relation to tree species diversity and its component factors, interspersion of different species and density of each tree species. Fifteen treatments of Douglas-fir (Pseudotsuga menziesii) and red alder (Alnus rubra) (various densities and proportions of each)were randomly assigned to 0.073 ha plots, replicated three-fold at each of two locations in Western Oregon: the Cascade Head Experimental Forest and the H. J. Andrews Experimental Forest. The six treatments used in this studywere two densities of Douglas-fir and red alder monoculture (1000 trees/ha and 500 trees/ha), and mixtures of Douglas-fir and red alder (500 trees/ha of each) planted simultaneouslyor red alder planted 6 years after the Douglas-fir. Trees were initially planted in 1985-1986. The arthropod communities were sampled in the summer of 1998 by bagging and pruning branches from the mid-canopy of both tree species. Multivariate analyses distinguished the arthropod communities foundon each tree species and geographical location, but not among the different diversity and density treatments. Many arthropod taxa and functional groups residingon a single tree species had significantly different abundances between locations. Themost commonly encountered taxon, Adelges cooleyi Gillette (Homoptera: Adelgidae),was most abundant on Douglas-firs in the 500 trees/ha monoculture and the mixture with younger red alder, and least abundant in the mixture with both species planted simultaneously (the1000 trees/ha Douglas-fir monoculture was intermediate). -
Evaluating a Standardized Protocol and Scale for Determining Non-Native Insect Impact
A peer-reviewed open-access journal NeoBiota 55: 61–83 (2020) Expert assessment of non-native insect impacts 61 doi: 10.3897/neobiota.55.38981 RESEARCH ARTICLE NeoBiota http://neobiota.pensoft.net Advancing research on alien species and biological invasions The impact is in the details: evaluating a standardized protocol and scale for determining non-native insect impact Ashley N. Schulz1, Angela M. Mech2, 15, Craig R. Allen3, Matthew P. Ayres4, Kamal J.K. Gandhi5, Jessica Gurevitch6, Nathan P. Havill7, Daniel A. Herms8, Ruth A. Hufbauer9, Andrew M. Liebhold10, 11, Kenneth F. Raffa12, Michael J. Raupp13, Kathryn A. Thomas14, Patrick C. Tobin2, Travis D. Marsico1 1 Arkansas State University, Department of Biological Sciences, PO Box 599, State University, AR 72467, USA 2 University of Washington, School of Environmental and Forest Sciences, 123 Anderson Hall, 3715 W Stevens Way NE, Seattle, WA 98195, USA 3 U.S. Geological Survey, Nebraska Cooperative Fish and Wildlife Unit, University of Nebraska-Lincoln, 423 Hardin Hall, 3310 Holdrege Street, Lincoln, NE 68583, USA 4 Dartmouth College, Department of Biological Sciences, 78 College Street, Hanover, NH 03755, USA 5 The University of Georgia, Daniel B. Warnell School of Forestry and Natural Resources, 180 E. Green St., Athens, GA 30602, USA 6 Stony Brook University, Department of Ecology and Evolution, Stony Brook, NY 11794, USA 7 USDA Forest Service Northern Research Station, 51 Mill Pond Rd., Hamden, CT 06514, USA 8 The Davey Tree Expert Company, 1500 N Mantua St., Kent, OH 44240, USA -
Widespread Occurrence of Black-Orange-Black Color Pattern in Hymenoptera
Journal of Insect Science, (2019) 19(2): 13; 1–12 doi: 10.1093/jisesa/iez021 Research Widespread Occurrence of Black-Orange-Black Color Pattern in Hymenoptera R. Mora1,2,3 and P. E. Hanson2 1Universidad de Costa Rica, Centro de Investigación en Biología Celular y Molecular, Ciudad de la Investigación Postal 11501-2060, San Pedro de Montes de Oca, SJ, Costa Rica, 2Universidad de Costa Rica, Escuela de Biología, Apartado Postal 11501-2060, San Pedro de Montes de Oca, SJ, Costa Rica, and 3Corresponding author, e-mail: [email protected] Subject Editor: Phyllis Weintraub Received 19 October 2018; Editorial decision 3 February 2019 Abstract Certain color patterns in insects show convergent evolution reflecting potentially important biological functions, for example, aposematism and mimicry. This phenomenon has been most frequently documented in Lepidoptera and Coleoptera, but has been less well investigated in Hymenoptera. It has long been recognized that many hymenopterans, especially scelionids (Platygastridae), show a recurring pattern of black head, orange/red mesosoma, and black metasoma (BOB coloration). However, the taxonomic distribution of this striking color pattern has never been documented across the entire order. The main objective of our research was to provide a preliminary tabulation of this color pattern in Hymenoptera, through examination of museum specimens and relevant literature. We included 11 variations of the typical BOB color pattern but did not include all possible variations. These color patterns were found in species belonging to 23 families of Hymenoptera, and was most frequently observed in scelionids, evaniids, and mutillids, but was relatively infrequent in Cynipoids, Diaprioids, Chalcidoids, and Apoids. -
Seasonal Variation in Honeydew Sugar Content of Galling Aphids (Aphidoidea: Pemphigidae: Fordinae) Feeding on Pistacia: Host Ecology and Aphid Physiology
ARTICLE IN PRESS Basic and Applied Ecology 7 (2006) 141—151 www.elsevier.de/baae Seasonal variation in honeydew sugar content of galling aphids (Aphidoidea: Pemphigidae: Fordinae) feeding on Pistacia: Host ecology and aphid physiology David Woola,Ã, Donald L. Hendrixb, Ofra Shukrya aDepartment of Zoology, Tel Aviv University, Tel Aviv 69978, Israel bWestern Cotton Research Laboratory, USDA-ARS, 4135 E Broadway Road, Phoenix, AZ 85040, USA Received 21 June 2004; accepted 25 February 2005 KEYWORDS Summary Aphid metabolism; We investigated the possibility that seasonal variation in host-tree sap quality was Gall aphids; reflected in aphid honeydew sugar content. Aphids (Homoptera) feed on the phloem Phloem feeding; sap of their host plants and excrete sugar-rich honeydew. We compared the sugar Seasonal changes composition of honeydew excreted by four species of closely related aphids (Pemphigidae: Fordinae ) inducing galls on Pistacia palaestina (Anacardiaceae). Samples were collected four times a year in 1997 and 1998. Samples from one species feeding on the roots of a secondary host, a perennial herb, were also included in the study. More than 20 sugars were detected in the honeydew. Sugars that were present in more than 40% of the samples were analyzed quantitatively in a hierarchical manner. The mean proportions of each sugar of the total sugar content in different species were not significantly different, but samples taken at different dates contained significantly different proportions of the sugars. The most frequent sugars in all species were glucose and fructose. Generally, the proportion of glucose exceeded fructose, but in honeydew from aphids feeding on the roots of the secondary host the reverse was true. -
Type Specimens of Aphids (Aphididae ; Homoptera) Described by M
TYPE SPECIMENS OF APHIDS (APHIDIDAE ; HOMOPTERA) DESCRIBED BY M. INOUYE IN THE Title HOKKAIDO UNIVERSITY INSECT COLLECTION Author(s) Sano, Masakazu Insecta matsumurana. New series : journal of the Faculty of Agriculture Hokkaido University, series entomology, 61, Citation 75-86 Issue Date 2005-02 Doc URL http://hdl.handle.net/2115/9923 Type bulletin (article) File Information 61_p75-86.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP INSECTA MATSUMURANA NEW SERIES 61: 75-86 FEBRUARY 2005 TYPE SPECIMENS OF APHIDS (APHIDIDAE; HOMOPTERA) DESCRIBED BY M. INOUYE IN THE HOKKAIDO UNIVERSITY INSECT COLLECTION By MASAKAZU SANO Abstract SANO, M. 2005. Type specimens of aphids (Aphididae; Homoptera) described by M. Inouye in the Hokkaido University Insect Collection. Ins. matsum. n. s. 61: 75-86. The aphid species, 18 in total, described by M. Inouye are listed. For IS species of them, their type specimens are confirmed to exist in the collection of Systematic Entomology, Hokkaido University. Collection data of the specimens and grounds for their confirmation are given. Author s address. Systematic Entomology, Graduate School of Agriculture, Hokkaido University, Sapporo, 060-8589 Japan. 75 INTRODUCTION Motonori Inouye (1901-1990) was a forest entomologist who provided the foundations for the taxonomy and control of conifer-feeding aphids in Japan. He described 18 species of Aphididae (Homoptera), mostly conifer-feeders, from Japan and Sakhalin as new to science. Dr. Inouye mentioned in his papers that the type specimens of these species were placed in several institutes he worked for at that time, although he sometimes did not indicate type depository.