Pinon Ips Bark Beetle
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
TREE NOTES CALIFORNIA DEPARTMENT of FORESTRY and FIRE PROTECTION Arnold Schwarzenegger Andrea E
TREE NOTES CALIFORNIA DEPARTMENT OF FORESTRY AND FIRE PROTECTION Arnold Schwarzenegger Andrea E. Tuttle Michael Chrisman Governor Director Secretary for Resources State of California The Resources Agency NUMBER: 28 JANUARY 2004 Ips Beetles in California Pines by Donald R. Owen Forest Pest Management Specialist, 6105 Airport Road, Redding, CA 96022 There are a number of bark beetle species that species, climate, and other factors, Ips may attack and kill pines in California. Foremost complete from one to many generations per among these are species of Dendroctonus and year. Under ideal conditions, a single Ips. Although species of Dendroctonus are generation may be completed in about 45 considered to be the most aggressive tree days. Ips killers, species of can be significant pests Ips under certain circumstances and/or on certain are shiny black to reddish brown, hosts. Nearly all of California’s native pines cylindrical beetles, ranging in size from about Ips 3 - 6.5 cm. A feature which readily areattackedbyoneormorespeciesof . Dendroctonus Some species of Ips also attack spruce, but are distinguishes them from beetles not considered to be significant pests in is the presence of spines on the posterior end California. of the wing covers. There may be between 3-6 pairs of spines, the size, number and While numerous bark beetles colonize pines, arrangement of which are unique for each only a handful are capable of killing live trees. The majority of bark beetles, including species of Ips, are secondary invaders that colonize recently dead, dying, or weakened trees. Those species of Ips that kill trees, do so opportunistically and typically only kill trees under stress. -
Bark Beetles
Bark Beetles O & T Guide [O-#03] Carol A. Sutherland Extension and State Entomologist Cooperative Extension Service z College of Agriculture and Home Economics z October 2006 Although New Mexico bark beetle adults are In monogamous species such as the Douglas small, rarely exceeding 1/3 inch in length, they fir beetle, Dendroctonus pseudotsugae, the are very capable of killing even the largest female bores the initial gallery into the host host trees with a mass assault, girdling them or tree, releases pheromones attractive to her inoculating them with certain lethal pathogens. species and accepts one male as her mate. Some species routinely attack the trunks and major limbs of their host trees, other bark beetle species mine the twigs of their hosts, pruning and weakening trees and facilitating the attack of other tree pests. While many devastating species of bark beetles are associated with New Mexico conifers, other species favor broadleaf trees and can be equally damaging. Scientifically: Bark beetles belong to the insect order Coleoptera and the family Scolytidae. Adult “engraver beetle” in the genus Ips. The head is on the left; note the “scooped out” area Metamorphosis: Complete rimmed by short spines on the rear of the Mouth Parts: Chewing (larvae and adults) beetle, a common feature for members of this Pest Stages: Larvae and adults. genus. Photo: USDA Forest Service Archives, USDA Forest Service, www.forestryimages.org Typical Life Cycle: Adult bark beetles are strong fliers and are highly receptive to scents In polygamous species such as the pinyon bark produced by damaged or stressed host trees as beetle, Ips confusus, the male bores a short well as communication pheromones produced nuptial chamber into the host’s bark, releases by other members of their species. -
And Pityogenes Knechteli (Swaine) (Coleoptera: Scolytidae) in Lodgepole Pine
" "SEMIOCHEMICAL-BASED COMMUNICATION IN INTERSPECIFIC INTERACTIONS BETWEEN IPS PINI (SAY) AND PITYOGENES KNECHTELI (SWAINE) (COLEOPTERA: SCOLYTIDAE) IN LODGEPOLE PINE . THERESE M. POLAND and JOHN H. BORDEN Centre forPest Management,Department of Biological Sciences, SimonFraser University, Bumaby, l BritishColumbia,Canada V5A 1S6 ,_._, _ ::._.., _.,.... Abstract The Canadian Entomologist 126:269-276 (1994) .,:.... _ , . , a The pine engraver, Ips pini Say, and Pityogenes knechteli Swaine often co-exist in " , lodgepole pine, Pinus contorta var. latifolia Engelmann. We tested the hypotheses that ,.. " P. knechteli produces an attractive pheromone and that the attraction of P. knechteli and _%_'.. • I. pini to conspecifics is inhibited by the presence of the other species. Pityogenes ._:,: knechteli males and females were attracted to bolts infested with conspecific males and •. , , to bolts infested with I. pini males; however, there was no significant cross-attraction of ...... •: _ - I. pini males or females to bolts infested with P. knechteli males. Attraction ofP. knechteli " :;• _ ..... ,and I. pini males and females to bolts infested with conspecific males was not inhibited • ,. ._ in the presence of bolts infested with males of the other bark beetle species. Pityogenes .... knechteli has no potential for compe.titive displacement of I. pini but may enhance the adverse effectof I. pini on.the mountain pine beetle, Dendroctonus ponderosae Hopkins. ; Poland, T.M., et J.H. Borden. 1994. Communication s6mio-chimique lors des interactions _e.. ., intersp6cifiquesentreIpspini (Say)et Pityogenesknechteli (Swaine) (Coleoptera:Scolytidae) " " chez le Pin de Murray.The Canadian Entomologist 126:269-276 ? R_sum_ • _ ' Les scolytes Ips pini Say et Pityogenes knechteli Swaine cohabitent souvent dans des ' '_7:.':_ ......:'_:_::'_ Pins de Murray Pinus contorta var. -
Spruce Beetle
QUICK GUIDE SERIES FM 2014-1 Spruce Beetle An Agent of Subalpine Change The spruce beetle is a native species in Colorado’s spruce forest ecosystem. Endemic populations are always present, and epidemics are a natural part of the changing forest. There usually are long intervals between such events as insect and disease epidemics and wildfires, giving spruce forests time to regenerate. Prior to their occurrence, the potential impacts of these natural disturbances can be reduced through proactive forest management. The spruce beetle (Dendroctonus rufipennis) is responsible for the death of more spruce trees in North America than any other natural agent. Spruce beetle populations range from Alaska and Newfoundland to as far south as Arizona and New Mexico. The subalpine Engelmann spruce is the primary host tree, but the beetles will infest any Figure 1. Engelmann spruce trees infested spruce tree species within their geographical range, including blue spruce. In with spruce beetles on Spring Creek Pass. Colorado, the beetles are most commonly observed in high-elevation spruce Photo: William M. Ciesla forests above 9,000 feet. At endemic or low population levels, spruce beetles generally infest only downed trees. However, as spruce beetle population levels in downed trees increase, usually following an avalanche or windthrow event – a high-wind event that topples trees over a large area – the beetles also will infest live standing trees. Spruce beetles prefer large (16 inches in diameter or greater), mature and over- mature spruce trees in slow-growing, spruce-dominated stands. However, at epidemic levels, or when large-scale, rapid population increases occur, spruce beetles may attack trees as small as 3 inches in diameter. -
Landscape Insect Pests of Concern
Utah’s Insect Pests of Concern: Fruit, Tree Borers, and Nuisance Western Horticultural Inspection Society, October 1, 2015 Diane Alston, Entomologist, Utah State University Some of the Tenacious Fruit and Nut Insect Pests Tephritid Fruit Flies ▪ ‘True’ fruit flies (~1/4 inch long) Apple Maggot: “F” ▪ 3 primary pest species in Utah Quarantine Pest ▪ Females have a sharp ovipositor to lay eggs under the skin of fruits & husks ▪ Susceptible when “soft enough”, e.g., blushed cherry Walnut Huskfly: ▪ Characteristic banding pattern on wings “Inverted V” ▪ Differentiate species ▪ Maggots tunnel in fruit ▪ Legless, cylindrical body (~1/4 inch long when full grown) Cherry Fruit Fly: ▪ Tapered head, 2 dark mouth hooks “Funky F & Small Window” Apple Maggot Native to Eastern North America: Primarily a Pest of Apple Egg-laying punctures in apple Larval tunnels in apple flesh Apple Maggot History in Utah ▪ Not currently a pest of commercial orchards ▪ Regulated as quarantine insect ▪ If established in commercial orchards, inflict substantial economic harm through loss of export markets ▪ First detected in western U.S. in Oregon in 1979; has spread in the PNW ▪ In Utah, first detected in cherry orchards in Mapleton (Utah Co.) in 1983 ▪ An extensive statewide survey in 1985 found it widely distributed in northern and west central UT ▪ River hawthorn (Crataegus rivularis Nutt.) ▪ Unmanaged cherries ▪ May be native to Utah (widely established) Apple Maggot in Utah - 2013 ▪ Home yard plum fruits ▪ River hawthorn nearby AM larva inside plum fruit ▪ No insecticide -
Seasonality and Lure Preference of Bark Beetles (Curculionidae: Scolytinae) and Associates in a Northern Arizona Ponderosa Pine Forest
COMMUNITY AND ECOSYSTEM ECOLOGY Seasonality and Lure Preference of Bark Beetles (Curculionidae: Scolytinae) and Associates in a Northern Arizona Ponderosa Pine Forest 1,2 1 3 1 M. L. GAYLORD, T. E. KOLB, K. F. WALLIN, AND M. R. WAGNER Environ. Entomol. 35(1): 37Ð47 (2006) ABSTRACT Ponderosa pine forests in northern Arizona have historically experienced limited bark beetle-caused tree mortality, and little is known about the bark beetle community in these forests. Our objectives were to describe the ßight seasonality and lure preference of bark beetles and their associates in these forests. We monitored bark beetle populations for 24 consecutive months in 2002 and 2003 using Lindgren funnel traps with Þve different pheromone lures. In both years, the majority of bark beetles were trapped between May and October, and the peak captures of coleopteran predator species, Enoclerus (F.) (Cleridae) and Temnochila chlorodia (Mannerheim), occurred between June and August. Trap catches of Elacatis (Coleoptera: Othniidae, now Salpingidae), a suspected predator, peaked early in the spring. For wood borers, trap catches of the Buprestidae family peaked in late May/early June, and catches of the Cerambycidae family peaked in July/August. The lure targeted for Dendroctonus brevicomis LeConte attracted the largest percentage of all Dendroc- tonus beetles except for D. valens LeConte, which was attracted in highest percentage to the lure targeted for D. valens. The lure targeted for Ips pini attracted the highest percentage of beetles for all three Ips species [I.pini (Say), I. latidens (LeConte), and I. lecontei Swaine] and the two predators, Enoclerus and T. chlorodia. -
Wayne National Forest Assessment
United States Department of Agriculture Assessment Wayne National Forest Forest Wayne National Forest Plan Service Forest Revision July 2020 Prepared By: Forest Service Wayne National Forest 13700 US Highway 33 Nelsonville, OH 45764 Responsible Official: Forest Supervisor Carrie Gilbert Abstract: The Assessment presents and evaluates existing information about relevant ecological, economic and social conditions, trends, risks to sustainability, and context within the broader landscape and relationship to the 2006 Wayne National Forest Land and Resource Management Plan (the forest plan). Cover Photo: The Wayne National Forest headquarters and welcome center. USDA photo by Kyle Brooks The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. In accordance with Federal civil rights law and U.S. Department of Agriculture (USDA) civil rights regulations and policies, the USDA, its Agencies, offices, and employees, and institutions participating in or administering USDA programs are prohibited from discriminating based on race, color, national origin, religion, sex, gender identity (including gender expression), sexual orientation, disability, age, marital status, family/parental status, income derived from a public assistance program, political beliefs, or reprisal or retaliation for prior civil rights activity, in any program or activity conducted or funded by USDA (not all bases apply to all programs). Remedies and complaint filing deadlines vary by program or incident. Persons with disabilities who require alternative means of communication for program information (e.g., Braille, large print, audiotape, American Sign Language, etc.) should contact the responsible Agency or USDA’s TARGET Center at (202) 720-2600 (voice and TTY) or contact USDA through the Federal Relay Service at (800) 877-8339. -
Evaluation of Screen Barriers on Redbay Trees to Protect Them From
Evaluation of Screen Barriers on Redbay Trees to Protect them from Xyleborus glabratus (Coleoptera: Curculionidae: Scolytinae) and Distribution of Initial Attacks in Relation to Stem Moisture Content, Diameter, and Height Author(s): M. Lake Maner , James L. Hanula , and S. Kristine Braman Source: Journal of Economic Entomology, 106(4):1693-1698. 2012. Published By: Entomological Society of America URL: http://www.bioone.org/doi/full/10.1603/EC13125 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. FOREST ENTOMOLOGY Evaluation of Screen Barriers on Redbay Trees to Protect Them From Xyleborus glabratus (Coleoptera: Curculionidae: Scolytinae) and Distribution -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
Fungi Associated with the North American Spruce Beetle, Dendroctonus Rufipennis
Color profile: Generic CMYK printer profile Composite Default screen 1815 NOTE / NOTE Fungi associated with the North American spruce beetle, Dendroctonus rufipennis Diana L. Six and Barbara J. Bentz Abstract: Fungi were isolated from individual Dendroctonus rufipennis (Kirby) collected from six populations in Alaska, Colorado, Utah, and Minnesota, U.S.A. In all populations, Leptographium abietinum (Peck) Wingfield was the most commonly isolated mycelial fungus (91–100% of beetles). All beetles in all populations were associated with yeasts and some with only yeasts (0–5%). In one population, Ophiostoma ips (Rumbold) Nannf. was also present on 5% of the beetles but always in combination with L. abietinum and yeasts. Ophiostoma piceae (Munch) H. & P. Sydow was found on 2% of beetles in another population. Ceratocystis rufipenni Wingfield, Harrington & Solheim, previously reported as an associate of D. rufipennis, was not isolated from beetles in this study. Ceratocystis rufipenni is a viru- lent pathogen of host Picea, which has led to speculation that C. rufipenni aids the beetle in overcoming tree defenses and therefore contributes positively to the overall success of the beetle during colonization. However, our results, con- sidered along with those of others, indicate that C. rufipenni may be absent from many populations of D. rufipennis and may be relatively rare in those populations in which it is found. If this is true, C. rufipenni may be only a minor or incidental associate of D. rufipennis and, as such, not likely to have significant impacts on beetle success or popula- tion dynamics. Alternatively, the rarity of C. rufipenni in our and others isolations may be due to difficulties in isolat- ing this fungus in the presence of other faster growing fungi such as L. -
(Coleoptera) from European Eocene Ambers
geosciences Review A Review of the Curculionoidea (Coleoptera) from European Eocene Ambers Andrei A. Legalov 1,2 1 Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences, Frunze Street 11, 630091 Novosibirsk, Russia; [email protected]; Tel.: +7-9139471413 2 Biological Institute, Tomsk State University, Lenina Prospekt 36, 634050 Tomsk, Russia Received: 16 October 2019; Accepted: 23 December 2019; Published: 30 December 2019 Abstract: All 142 known species of Curculionoidea in Eocene amber are documented, including one species of Nemonychidae, 16 species of Anthribidae, six species of Belidae, 10 species of Rhynchitidae, 13 species of Brentidae, 70 species of Curcuionidae, two species of Platypodidae, and 24 species of Scolytidae. Oise amber has eight species, Baltic amber has 118 species, and Rovno amber has 16 species. Nine new genera and 18 new species are described from Baltic amber. Four new synonyms are noted: Palaeometrioxena Legalov, 2012, syn. nov. is synonymous with Archimetrioxena Voss, 1953; Paleopissodes weigangae Ulke, 1947, syn. nov. is synonymous with Electrotribus theryi Hustache, 1942; Electrotribus erectosquamata Rheinheimer, 2007, syn. nov. is synonymous with Succinostyphlus mroczkowskii Kuska, 1996; Protonaupactus Zherikhin, 1971, syn. nov. is synonymous with Paonaupactus Voss, 1953. Keys for Eocene amber Curculionoidea are given. There are the first records of Aedemonini and Camarotini, and genera Limalophus and Cenocephalus in Baltic amber. Keywords: Coleoptera; Curculionoidea; fossil weevil; new taxa; keys; Palaeogene 1. Introduction The Curculionoidea are one of the largest and most diverse groups of beetles, including more than 62,000 species [1] comprising 11 families [2,3]. They have a complex morphological structure [2–7], ecological confinement, and diverse trophic links [1], which makes them a convenient group for characterizing modern and fossil biocenoses. -
Wingnut (Juglandaceae)
83 Wingnut (Juglandaceae) as a new generic host for Pityophthorus juglandis (Coleoptera: Curculionidae) and the thousand cankers disease pathogen, Geosmithia morbida (Ascomycota: Hypocreales) Stacy M. Hishinuma, Paul L. Dallara, Mohammad A. Yaghmour, Marcelo M. Zerillo, Corwin M. Parker, Tatiana V. Roubtsova, Tivonne L. Nguyen, Ned A. Tisserat, Richard M. Bostock, Mary L. Flint, Steven J. Seybold1 Abstract—The walnut twig beetle (WTB), Pityophthorus juglandis Blackman (Coleoptera: Curculionidae), vectors a fungus, Geosmithia morbida Kolařík, Freeland, Utley, and Tisserat (Ascomycota: Hypocreales), which colonises and kills the phloem of walnut and butternut trees, Juglans Linnaeus (Juglandaceae). Over the past two decades, this condition, known as thousand cankers disease (TCD), has led to the widespread mortality of Juglans species in the United States of America. Recently the beetle and pathogen were discovered on several Juglans species in northern Italy. Little is known about the extra-generic extent of host acceptability and suitability for the WTB. We report the occurrence of both the WTB and G. morbida in three species of wingnut, Pterocarya fraxinifolia Spach, Pterocarya rhoifolia Siebold and Zuccarini, and Pterocarya stenoptera de Candolle (Juglandaceae) growing in the United States Department of Agriculture-Agricultural Research Service, National Clonal Germplasm Repository collection in northern California (NCGR) and in the Los Angeles County Arboretum and Botanic Garden in southern California, United States of America. In two instances (once in P. stenoptera and once in P. fraxinifolia) teneral (i.e., brood) adult WTB emerged and were collected more than four months after infested branch sections had been collected in the field. Koch’s postulates were satisfied with an isolate of G.