Elm Bark Beetles Native and Introduced Bark Beetles of Elm
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Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Papers in Entomology Museum, University of Nebraska State 12-2009 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson Wichita State University, [email protected] Darcy E. Oishi 2Hawaii Department of Agriculture, Plant Pest Control Branch, Honolulu, [email protected] Brett C. Ratcliffe University of Nebraska-Lincoln, [email protected] Grant T. McQuate USDA-ARS-PBARC, U.S. Pacific Basin Agricultural Research Center, Hilo, HI, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/entomologypapers Part of the Entomology Commons Jameson, Mary Liz; Oishi, Darcy E.; Ratcliffe, Brett C.; and McQuate, Grant T., "Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii" (2009). Papers in Entomology. 147. https://digitalcommons.unl.edu/entomologypapers/147 This Article is brought to you for free and open access by the Museum, University of Nebraska State at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. AProcddition. HawaiianAl inv AEsiventomol scA.r SAocbs. in(2009) HAwA 41:25–30ii 25 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson1, Darcy E. Oishi2, Brett C. Ratcliffe3, and Grant T. McQuate4 1Wichita State University, Department of Biological Sciences, 537 Hubbard Hall, Wichita, Kansas 67260 [email protected]; 2Hawaii Department of Agriculture, Plant Pest Control Branch, 1428 South King St., Honolulu, HI 96814 [email protected]; 3University of Nebraska State Museum, Systematics Research Collections, W436 Nebraska Hall, University of Nebraska, Lincoln, Nebraska 68588 [email protected]; 4USDA-ARS-PBARC, U.S. -
Biology and Management of the Dutch Elm Disease Vector, Hylurgopinus Rufipes Eichhoff (Coleoptera: Curculionidae) in Manitoba By
Biology and Management of the Dutch Elm Disease Vector, Hylurgopinus rufipes Eichhoff (Coleoptera: Curculionidae) in Manitoba by Sunday Oghiakhe A thesis submitted to the Faculty of Graduate Studies of The University of Manitoba in partial fulfilment of the requirements of the degree of Doctor of Philosophy Department of Entomology University of Manitoba Winnipeg Copyright © 2014 Sunday Oghiakhe Abstract Hylurgopinus rufipes, the native elm bark beetle (NEBB), is the major vector of Dutch elm disease (DED) in Manitoba. Dissections of American elms (Ulmus americana), in the same year as DED symptoms appeared in them, showed that NEBB constructed brood galleries in which a generation completed development, and adult NEBB carrying DED spores would probably leave the newly-symptomatic trees. Rapid removal of freshly diseased trees, completed by mid-August, will prevent spore-bearing NEBB emergence, and is recommended. The relationship between presence of NEBB in stained branch sections and the total number of NEEB per tree could be the basis for methods to prioritize trees for rapid removal. Numbers and densities of overwintering NEBB in elm trees decreased with increasing height, with >70% of the population overwintering above ground doing so in the basal 15 cm. Substantial numbers of NEBB overwinter below the soil surface, and could be unaffected by basal spraying. Mark-recapture studies showed that frequency of spore bearing by overwintering beetles averaged 45% for the wild population and 2% for marked NEBB released from disease-free logs. Most NEBB overwintered close to their emergence site, but some traveled ≥4.8 km before wintering. Studies comparing efficacy of insecticides showed that chlorpyrifos gave 100% control of overwintering NEBB for two years as did bifenthrin: however, permethrin and carbaryl provided transient efficacy. -
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. -
Dutch Elm Disease Pathogen Transmission by the Banded Elm Bark Beetle Scolytus Schevyrewi
For. Path. 43 (2013) 232–237 doi: 10.1111/efp.12023 © 2013 Blackwell Verlag GmbH Dutch elm disease pathogen transmission by the banded elm bark beetle Scolytus schevyrewi By W. R. Jacobi1,3, R. D. Koski1 and J. F. Negron2 1Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins, CO 80523, USA; 2U.S.D.A. Forest Service, Rocky Mountain Forest Research Station, Fort Collins, CO USA; 3E-mail: [email protected] (for correspondence) Summary Dutch Elm Disease (DED) is a vascular wilt disease of Ulmus species (elms) incited in North America primarily by the exotic fungus Ophios- toma novo-ulmi. The pathogen is transmitted via root grafts and elm bark beetle vectors, including the native North American elm bark beetle, Hylurgopinus rufipes and the exotic smaller European elm bark beetle, Scolytus multistriatus. The banded elm bark beetle, Scolytus schevyrewi, is an exotic Asian bark beetle that is now apparently the dominant elm bark beetle in the Rocky Mountain region of the USA. It is not known if S. schevyrewi will have an equivalent vector competence or if management recommendations need to be updated. Thus the study objectives were to: (i) determine the type and size of wounds made by adult S. schevyrewi on branches of Ulmus americana and (ii) determine if adult S. schevyrewi can transfer the pathogen to American elms during maturation feeding. To determine the DED vectoring capability of S. schevyrewi, newly emerged adults were infested with spores of Ophiostoma novo-ulmi and then placed with either in-vivo or in-vitro branches of American elm trees. -
Mountain Pine Beetle Voltinism and Life History Characteristics Across Latitudinal and Elevational Gradients in the Western United States
For. Sci. 60(3):434–449 FUNDAMENTAL RESEARCH http://dx.doi.org/10.5849/forsci.13-056 entomology & pathology Mountain Pine Beetle Voltinism and Life History Characteristics across Latitudinal and Elevational Gradients in the Western United States Barbara Bentz, James Vandygriff, Camille Jensen, Tom Coleman, Patricia Maloney, Sheri Smith, Amanda Grady, and Greta Schen-Langenheim Substantial genetic variation in development time is known to exist among mountain pine beetle (Dendroctonus ponderosae Hopkins) populations across the western United States. The effect of this variation on geographic patterns in voltinism (generation time) and thermal requirements to produce specific voltinism pathways have not been investigated. The influence of voltinism on fitness traits, body size, and sex ratio is also unclear. We monitored mountain pine beetle voltinism, adult body size, sex ratio, and air temperatures at sites across latitudinal and elevational gradients in the western United States. With the exception of two sites at the coolest and warmest locations, the number of days required to complete a generation was similar. Thermal units required to achieve a generation, however, were significantly less for individuals at the coolest sites. Evolved adaptations explain this pattern, including developmental rates and thresholds that serve to synchronize cohorts and minimize cold-sensitive life stages in winter. These same adaptations reduce the capacity of mountain pine beetle at the warmest sites to take full advantage of increased thermal units, limiting the capacity for bivoltinism within the current realized distribution. Temperature was not correlated with adult size and sex ratio, and size was greatest in host trees other than lodgepole pine (Pinus contorta Dougl.). -
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. -
Leptographium Wageneri
Leptographium wageneri back stain root disease Dutch elm disease and Scolytus multistriatus DED caused the death of millions of elms in Europe and North America from around 1920 through the present Dutch Elm Disease epidemics in North America Originally thought one species of Ophiostoma, O. ulmi with 3 different races Now two species are recognized, O. ulmi and O. novo-ulmi, and two subspecies of O. novo-ulmi Two nearly simultaneous introductions in North America and Europe 1920s O. ulmi introduced from Europe, spread throughout NA, but caused little damage to native elm trees either in NA or Europe 1950s, simultaneous introductions of O. novo-ulmi, Great Lakes area of US and Moldova-Ukraine area of Europe. North American and Europe subspecies are considered distinct. 1960 NA race introduced to Europe via Canada. By 1970s much damage to US/Canada elms killed throughout eastern and central USA O. novo-ulmi has gradually replaced O. ulmi in both North America and Europe more fit species replacing a less fit species O. novo-ulmi able to capture greater proportion of resource O. novo-ulmi probably more adapted to cooler climate than O. ulmi During replacement, O. ulmi and O. novo-ulmi occur in close proximity and can hybridize. Hybrids are not competitive, but may allow gene flow from O. ulmi to O. novo-ulmi by introgression: Backcrossing of hybrids of two plant populations to introduce new genes into a wild population Vegetative compatibility genes heterogenic incompatibility multiple loci prevents spread of cytoplasmic viruses O. novo-ulmi arrived as a single vc type, but rapidly acquired both new vc loci AND virus, probably from hybridizing with O. -
Siberian Elm Ulmus Pumila ILLINOIS RANGE Tree
Siberian elm Ulmus pumila Kingdom: Plantae FEATURES Division: Magnoliophyta Siberian elm is also known as Chinese elm. This Class: Magnoliopsida deciduous shrub or small tree may grow to a height Order: Urticales of 35 feet and a trunk diameter of one foot. Leaves are in an alternate arrangement along the stem. The Family: Ulmaceae simple leaves average about one to three inches in ILLINOIS STATUS length and are single-toothed. A short leafstalk is present at the base of the leaf. The buds are red- common, nonnative brown and blunt. Each spherical, hairy bud is about © Guy Sternberg one-eighth inch in diameter. The bark of this tree is gray or brown with shallow furrows. Thin, smooth twigs may be brown or gray. Flowers are borne in drooping clusters of two to five, appearing before the leaves begin to unfold. These small, green flowers have no petals. The fruit is a samara, a winged seed. The samara is round, smooth and one- seeded. Each samara is about one-half inch in diameter. BEHAVIORS Siberian elm may be found statewide in Illinois. It grows in waste areas. Flowers are produced in May. Wind is the main agent of pollination and seed dispersal. Its pale, brown wood is hard and heavy. Siberian elm is grown as an ornamental tree and is tree often found around old buildings. Some escapes from these plantings have established themselves in ILLINOIS RANGE the wild. Siberian elm is a native of Asia. © Illinois Department of Natural Resources. 2021. Biodiversity of Illinois. Unless otherwise noted, photos and images © Illinois Department of Natural Resources. -
Darkling Beetles and Mealworms Theresa A
Darkling Beetles and Mealworms Theresa A. Dellinger and Eric R. Day, Department of Entomology, Virginia Tech Description Darkling beetles belong in the beetle family Tenebrionidae, which consists of more than 20,000 species of beetles. Adult darkling beetles widely range in shape and size, with most measuring from 2 – 19 mm (0.13” – 0.75”). Adults are usually a reddish-brown to brownish-black in color and can be shiny or dull. The elytra (the wing covers) can be smooth, grooved, or otherwise sculptured. Most do not have colorful patterns on their wing covers. Adults are most active at night and tend to avoid bright lights. Darkling beetle larvae are often referred to as mealworms or false wireworms. They are long, hard-bodied grubs with a cylindrical shape and are shiny yellow-brown to darKer brown in color. They are active crawlers. Yellow mealworm larva, top. Dark mealworm larva, bottom. Clemson University-USDA Cooperative Adult yellow mealworm, Tenebrio molitor. Extension Slide Series, Bugwood.org. Clemson University-USDA Cooperative Extension Slide Series, Bugwood.org. Life Cycle Darkling beetles have a complete life cycle with egg, larval, pupal, and adult stages. Most species of darkling beetles have a slow rate of development and may live for a year as an adult. Species living on grains or other stored products may develop faster. Habitat/Distribution Darkling beetles are found throughout the world except for places with very cold climates. They are scavengers and omnivores, feeding on decomposing plant material, dead insects, fungi, and stored products. Only a handful of darkling beetles are considered pests; the vast majority of them live in the wild and pose no harm. -
Invasive Species: a Challenge to the Environment, Economy, and Society
Invasive Species: A challenge to the environment, economy, and society 2016 Manitoba Envirothon 2016 MANITOBA ENVIROTHON STUDY GUIDE 2 Acknowledgments The primary author, Manitoba Forestry Association, and Manitoba Envirothon would like to thank all the contributors and editors to the 2016 theme document. Specifically, I would like to thank Robert Gigliotti for all his feedback, editing, and endless support. Thanks to the theme test writing subcommittee, Kyla Maslaniec, Lee Hrenchuk, Amie Peterson, Jennifer Bryson, and Lindsey Andronak, for all their case studies, feedback, editing, and advice. I would like to thank Jacqueline Montieth for her assistance with theme learning objectives and comments on the document. I would like to thank the Ontario Envirothon team (S. Dabrowski, R. Van Zeumeren, J. McFarlane, and J. Shaddock) for the preparation of their document, as it provided a great launch point for the Manitoba and resources on invasive species management. Finally, I would like to thank Barbara Fuller, for all her organization, advice, editing, contributions, and assistance in the preparation of this document. Olwyn Friesen, BSc (hons), MSc PhD Student, University of Otago January 2016 2016 MANITOBA ENVIROTHON STUDY GUIDE 3 Forward to Advisors The 2016 North American Envirothon theme is Invasive Species: A challenge to the environment, economy, and society. Using the key objectives and theme statement provided by the North American Envirothon and the Ontario Envirothon, the Manitoba Envirothon (a core program of Think Trees – Manitoba Forestry Association) developed a set of learning outcomes in the Manitoba context for the theme. This document provides Manitoba Envirothon participants with information on the 2016 theme. -
Lacebark Elm Cultivars Ulmus Parvifolia
Lacebark Elm Cultivars Ulmus parvifolia P O Box 189 | Boring OR 97009 | 800-825-8202 | www.jfschmidt.com Ulmus parvifolia ‘Emer II’ PP 7552 Tall, upright and arching, this cultivar’s growth habit is unique Allee® Elm among U. parvifolia cultivars, Zone: 5 | Height: 50' | Spread: 35' being reminiscent of the grand Shape: Upright vase, arching American Elm. Its exfoliating Foliage: Medium green, glossy bark creates a mosaic of orange, Fall Color: Yellow-orange to rust red tan and gray, a beautiful sight on a mature tree. Discovered by DISEASE TOLERANCE: Dr. Michael Dirr of University of Dutch Elm Disease and phloem Georgia, Athens. necrosis Ulmus parvifolia ‘Emer I’ Bark of a mature tree is a mosaic of orange, tan, and gray patches, Athena® Classic Elm giving it as much interest in winter Zone: 5 | Height: 30' | Spread: 35' as in summer. The canopy is tightly Shape: Broadly rounded formed. Discovered by Dr. Michael Foliage: Medium green, glossy Dirr of University of Georgia, Fall Color: Yellowish Athens. DISEASE TOLERANCE: Dutch Elm Disease and phloem necrosis Ulmus parvifolia ‘UPMTF’ PP 11295 Bosque® is well shaped for plant- ing on city streets and in restricted Bosque® Elm spaces, thanks to its upright Zone: 6 | Height: 45' | Spread: 30' growth habit and narrow crown. Shape: Upright pyramidal to Fine textured and glossy, its dark broadly oval green foliage is complemented by Foliage: Dark green, glossy multi-colored exfoliating bark. Fall Color: Yellow-orange DISEASE TOLERANCE: Dutch Elm Disease and phloem necrosis Ulmus parvifolia ‘Dynasty’ A broadly rounded tree with fine textured foliage and good Dynasty Elm environ mental tolerance. -
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