Biological Control of Southern Pine Beetle Fred M

Total Page:16

File Type:pdf, Size:1020Kb

Biological Control of Southern Pine Beetle Fred M Biological Control of Southern Pine Beetle Fred M. Stephen1 and C. Wayne Berisford2 1Professor, Department of Entomology, University of Arkansas, Fayetteville, AR 72701 28 2Emeritus Professor, Department of Entomology, University of Georgia, Athens, GA 30602 Abstract Exotic invasive forest insects are frequently managed through classical biological control, which involves searching for, introducing, and establishing their exotic natural enemies. Biological control of native bark beetles, including the southern pine beetle (SPB), has been primarily attempted by conserving and manipulating their natural enemies. Knowledge of the role and biology of SPB natural enemies is increasing but is still limited, and is rarely well connected to coincident estimates of SPB host density. A rich complex of SPB native natural enemies exists, and these are discussed in greater detail in other chapters in this book. The cryptic nature of Dendroctonus species within phloem and bark, combined with the properties of many natural enemies (small size, highly aggregated distribution, lower density than their prey, and often acting late in the beetle’s life cycle), results in challenging sampling problems that are difficult to overcome. Attempts to assess impact of natural enemies have often been presented as percent Keywords of mortality, but rarely do these assessments show variation in mortality. The manner in which mortality varies with host density is important in population bark beetles regulation. Predators, parasitoids, and competitors of the SPB respond in varying parasitoid competitors degrees to SPB pheromones and tree volatiles during host selection. Variables population dynamics such as bark thickness and SPB density influence parasitoid success. In making predators oviposition choices, parasitoids tend to select the host beetle and tree species Scolytidae from which they emerged. Short SPB generation times, continuous flight, and attack by SPB adults result in infestations containing all life stages of beetles and natural enemies. Opportunities for numerical response of parasitoids to epidemic population growth should be great but have not been confirmed. Manipulation efforts indicate that providing nutrients for parasitoid adults increases their longevity, stimulates production of additional eggs, and prevents resorption of existing eggs. Parasitoids do forage in canopies of both pine and hardwood trees, possibly to acquire honeydew as adult nutrition. Predators frequently are the most abundant and visible sources of SPB mortality, and their potential role as delayed density-dependent agents may be important in the cycles exhibited by SPB populations. Simulation models that experimentally remove mortality attributable to natural enemies show how rapidly infestations grow when natural enemies are absent. Experimental research on Monochamus spp. indicates that they can cause high mortality to SPB brood as competitors and predators, and field observations suggest that they may play an important role in the collapse of SPB epidemics. 415 28.1.INTRODUCTION best definition is that of DeBach (1964), who considers biological control as a phase of natural Infestations of southern pine beetle control and defines it “as the action of parasites, (Dendroctonus frontalis Zimmermann) (SPB) predators, or pathogens in maintaining another are a veritable hive of insect activity, and organism’s population density at a lower the majority of these insects are not SPBs. average than would occur in their absence.” At Observations from a field-based perspective of its core, this definition implies that biological climbing hundreds of infested trees, sampling control is a natural process. The native complex bark that contains different SPB life stages, of predators, parasitoids, and competitors and studying the multitudes of insect species associated with the SPB, for example, reduces searching on the bark surface and burrowing and to some extent SPB population density. This developing within the inner bark and phloem, does not necessarily imply that natural enemies reveal the remarkable diversity of the SPB- will maintain SPB population density below associate complex. Many of these associated a level that is economically acceptable, but it insects parasitize, prey upon, or compete for does mean that without these natural enemies food and/or space with the SPB, and as such are the SPB would be a more significant pest. considered natural enemies of the beetle. In five other chapters of this book detailed information 28.2.2.TheFieldofBiological is presented on SPB predators (chapter 10), Control parasitoids (chapter 8), competitors (chapter 12), and fungal and mite associates (chapters Biological control of insect pests can be 9 and 11). Despite the extensive information considered an applied discipline; however, its that is known about SPB natural enemies, it is foundations are based in ecological theory. Thus safe to say that we still know much less than knowledge of insect ecology and ecosystem we should about their roles and importance interactions is usually key to successful in suppressing SPB population density. The biological control. Although much is known, purpose of this chapter is to define the field of we still do not have sufficient knowledge to biological control as it relates to the SPB and enact successful biological programs against the to briefly summarize attempts made at SPB SPB. Biological control as a discipline is often biological control. separated by the origins of pests and of their natural enemies and by the approaches used to maximize the effectiveness of the natural enemies. These approaches can be distinguished 28.2.Biological control as follows: 1. classical biological control – the Human manipulation of natural enemies to importation and establishment of exotic natural effect reduction of pest populations has existed enemies to control exotic or native pests; and for millennia; however, the term “biological 2. manipulative biological control – techniques control” was first used by H.S. Smith (1919) that manipulate natural enemies to augment to signify use of natural enemies, whether or enhance their effectiveness, or techniques introduced or not, to control insect pests. that manipulate the environment to benefit and Successful biological control of forest insects conserve existing natural enemies. Examples is well documented (Dahlsten and Mills 1999, of these approaches in relation to the SPB are Dahlsten and Whitmore 1989, Pschorn-Walcher explained and discussed below. Disruption of 1977, Turnock and others 1976, Waters and naturally occurring biological control through others 1976), and biological control is today a human intervention can and does occur. This primary tactic for management of many exotic knowledge should further stimulate our efforts forest insect pests. to gain more knowledge of forest / bark beetle / natural enemy interactions. Because 28.2.1.Definitions successful biological control must be based on Natural control is a broad concept that the fundamentals of scientific knowledge, it is encompasses the combined actions of abiotic essential to subsequently evaluate the reasons and/or biotic environmental factors to maintain for success or failure of biological control an organism’s more or less fluctuating programs. population density, within certain definable upper and lower limits, over a period of time Importation (Classical Biological (DeBach 1964). Although the term “biological Control) control” is used in many ways by different The importation of natural enemies to control authors, the most accepted and in our view the exotic (introduced) pests is by far the most 416 Stephen | Berisford common approach to biological control of forest and conserving natural enemies is for native insects (Dahlsten and Mills 1999). Invasive pests a strategy more important and more likely insects or other organisms that are accidentally to succeed. Humans can act to augment numbers or intentionally introduced from geographically of natural enemies, and they can manipulate distant areas into a new locale such as North their habitats so as to increase natural enemy America may reproduce without mortality from survival and effectiveness. Actions that natural enemies or host resistance that normally manipulate insects themselves can theoretically evolves through generations of insect-plant be considered distinct from actions that alter the interactions. The search for natural enemies of environment in which the insects live; however, the pest in its native area, coupled with their in practice it can be difficult to distinguish the importation, quarantined rearing to eliminate two (Rabb and others 1976). Conservation of secondary parasitoids or diseases, in concert natural enemies may be an approach that is with release, establishment, and control of the highly appropriate in forest ecosystems, as they pest in its new environment constitutes classical are longer lived, suffer fewer disruptions, and biological control (DeBach 1964). In forest are generally more complex than agricultural systems, classical biological control should be systems (Dahlsten and Mills 1999). considered as an essential management tool, particularly in light of the increasing numbers Study of invasive exotic pest species that are being The phrase, “know your enemy,” would seem discovered. If eradication of these exotic species to be essential to any commander of a military fails, then management of their populations campaign, and may be an appropriate
Recommended publications
  • 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.
    [Show full text]
  • 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.).
    [Show full text]
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • Host Plant Volatiles for Herbivores: a Bypass-Trophic Signal
    Inhibition of Predator Attraction to Kairomones by Non- Host Plant Volatiles for Herbivores: A Bypass-Trophic Signal Qing-He Zhang¤, Fredrik Schlyter* Chemical Ecology, Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Alnarp, Sweden Abstract Background: Insect predators and parasitoids exploit attractive chemical signals from lower trophic levels as kairomones to locate their herbivore prey and hosts. We hypothesized that specific chemical cues from prey non-hosts and non-habitats, which are not part of the trophic chain, are also recognized by predators and would inhibit attraction to the host/prey kairomone signals. To test our hypothesis, we studied the olfactory physiology and behavior of a predaceous beetle, Thanasimus formicarius (L.) (Coleoptera: Cleridae), in relation to specific angiosperm plant volatiles, which are non-host volatiles (NHV) for its conifer-feeding bark beetle prey. Methodology/Principal Findings: Olfactory detection in the clerid was confirmed by gas chromatography coupled to electroantennographic detection (GC-EAD) for a subset of NHV components. Among NHV, we identified two strongly antennally active molecules, 3-octanol and 1-octen-3-ol. We tested the potential inhibition of the combination of these two NHV on the walking and flight responses of the clerid to known kairomonal attractants such as synthetic mixtures of bark beetle (Ips spp.) aggregation pheromone components (cis-verbenol, ipsdienol, and E-myrcenol) combined with conifer (Picea and Pinus spp.) monoterpenes (a-pinene, terpinolene, and D3-carene). There was a strong inhibitory effect, both in the laboratory (effect size d = 23.2, walking bioassay) and in the field (d = 21.0, flight trapping). This is the first report of combining antennal detection (GC-EAD) and behavioral responses to identify semiochemical molecules that bypass the trophic system, signaling habitat information rather than food related information.
    [Show full text]
  • Altitudinal Variation of Dung Beetle (Scarabaeidae: Scarabaeinae
    Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2005) 14, 327–337 Blackwell Publishing, Ltd. RESEARCH Altitudinal variation of dung beetle PAPER (Scarabaeidae: Scarabaeinae) assemblages in the Colombian Andes Federico Escobar1,2,*, Jorge M. Lobo3 and Gonzalo Halffter1 1Departamento de Biodiversidad y ABSTRACT Comportamiento Animal, Instituto de Ecología, Aim We describe the changes in species richness, rarity and composition with alti- A.C., Apartado Postal 63, 91000 Xalapa, tude, and explore whether the differences in Scarabaeinae dung beetle composition Veracruz, México; 2Programa de Inventarios de Biodiversidad, Instituto Humboldt, Apartado along five altitudinal transects of the same mountain range are related to altitude or Aéreo 8693 Santafé de Bogotá, Colombia; and if there are interregional differences in these altitudinal gradients. 3 Departamento de Biodiversidad y Biología Location Field work was carried out on the eastern slope of the eastern Cordillera, Evolutiva, Museo Nacional de Ciencias Colombian Andes, between Tamá Peak to the north, in the Tamá National Park Naturales (CSIC), c/José Gutiérrez Abascal, 2. (07°23′ N, 72°23′ W) and the San Miguel River (00°28′ N, 77°17′ W) to the south. E-28006 Madrid, Spain Methods Sampling was carried out between February 1997 and November 1999 in five regions spanning elevation gradients. In each gradient, six sites were chosen at 250 m intervals between 1000 and 2250 m a.s.l. Results We found a curvilinear relationship between altitude and mean species rich- ness, with a peak in richness at middle elevations. However, the diversity of dung beetle assemblages does not seem to be related to the interregional differences in environ- mental conditions.
    [Show full text]
  • Functional Evolution of a Bark Beetle Odorant Receptor Clade Detecting Monoterpenoids of Different Ecological Origins
    bioRxiv preprint doi: https://doi.org/10.1101/2020.12.28.424525; this version posted December 28, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Functional evolution of a bark beetle odorant receptor clade detecting monoterpenoids of different ecological origins Xiao-Qing Hou1, Jothi Kumar Yuvaraj1, Rebecca E. Roberts1, C. Rikard Unelius2, Christer Löfstedt1, Martin N. Andersson1* 1Department of Biology, Lund University, Lund, Sweden 2 Faculty of Health and Life Sciences, Linnaeus University, Kalmar, Sweden *Corresponding author: Martin N. Andersson Department of Biology, Sölvegatan 37, 223 62 Lund, Sweden. Email: [email protected] Phone: +46-(0)462229344 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.12.28.424525; this version posted December 28, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Insects detect odors using an array of odorant receptors (ORs), which may expand through gene duplication. How specificities evolve and new functions arise in related ORs within a species remain poorly investigated. We addressed this question by functionally characterizing ORs from the Eurasian spruce bark beetle Ips typographus, in which antennal detection and behavioral responses to pheromones, volatiles from host and non-host trees, and fungal symbionts are well described.
    [Show full text]
  • DARKLING BEETLE Or STINK BEETLE Class Order Family Genus Species Insecta Coleoptera Tenebrionidae Eleodes Spp
    DARKLING BEETLE or STINK BEETLE Class Order Family Genus Species Insecta Coleoptera Tenebrionidae Eleodes spp Range: Found worldwide. 100 species in this genus in California. Habitat: Forests, grasslands, and deserts. Found under rocks and logs during the day. Niche: Herbivorous, terrestrial, nocturnal Diet: Wild: Scavenge on a wide variety of decaying and fresh plant and animal matter Zoo: Apple, monkey chow, lettuce Special Adaptations: The forewing (elytra) is fused so this beetle is flightless. They have chewing mouthparts and adults have a hard exoskeleton, smooth and black and are a little over an inch long. Antennae are thread-like, but some species’ are slightly enlarged at the terminal end and appear club-like. Darkling beetles undergo a complete metamorphosis. The eggs are laid in soil. The mealworm is the larval state of the darkling beetle and may molt 9-20 times. The adults will live 3-15 years. Compound eyes are kidney-shaped or notched rather than round. These beetles do not need to drink and can produce water metabolically; also their wings are fused to reduce water loss. Other: When disturbed, they will stand on their heads and elevate their rear end and emit a foul-smelling odor. This emission makes them unpalatable to would-be predators. Hence an alternate common name of “stink beetle”. They are sexually dimorphic. The cactus longhorn beetle mimics the darkling beetle because of the smell. Complete metamorphosis. ▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼▲▼ DERMESTID BEETLE or SKIN BEETLE Class Order Family Genus Species Insecta Coleoptera Dermestidae Dermestes maculatus Range: Worldwide distribution except Antarctica Habitat: on dead animals Niche: Scavengers, omnivorous, terrestrial Diet: Wild: dry animal or plant material such as skin or pollen, animal hair, feathers, dead insects and natural fibers Zoo: Special Adaptations: Undergo complete metamorphosis.
    [Show full text]
  • The Biodiversity of Flying Coleoptera Associated With
    THE BIODIVERSITY OF FLYING COLEOPTERA ASSOCIATED WITH INTEGRATED PEST MANAGEMENT OF THE DOUGLAS-FIR BEETLE (Dendroctonus pseudotsugae Hopkins) IN INTERIOR DOUGLAS-FIR (Pseudotsuga menziesii Franco). By Susanna Lynn Carson B. Sc., The University of Victoria, 1994 A THESIS SUBMITTED IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in THE FACULTY OF GRADUATE STUDIES (Department of Zoology) We accept this thesis as conforming To t(p^-feguired standard THE UNIVERSITY OF BRITISH COLUMBIA 2002 © Susanna Lynn Carson, 2002 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. 1 further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department The University of British Columbia Vancouver, Canada DE-6 (2/88) Abstract Increasing forest management resulting from bark beetle attack in British Columbia's forests has created a need to assess the impact of single species management on local insect biodiversity. In the Fort St James Forest District, in central British Columbia, Douglas-fir (Pseudotsuga menziesii Franco) (Fd) grows at the northern limit of its North American range. At the district level the species is rare (representing 1% of timber stands), and in the early 1990's growing populations of the Douglas-fir beetle (Dendroctonus pseudotsuage Hopkins) threatened the loss of all mature Douglas-fir habitat in the district.
    [Show full text]
  • 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.
    [Show full text]
  • Checkered Beetle Thanasimus Dubius (Fabricius)
    adult larva The Bugwood Network and USDA Forest Service adult larva The Bugwood Network and USDA Forest Service checkered beetle Thanasimus dubius (Fabricius) Checkered beetles in the family Cleridae are among the most important insect predators attacking forest insect pests. Adults of most species are active, antlike, brightly colored, hairy beetles that prey on adult beetles. Larvae live in the galleries and tunnels of bark beetles and woodborers and destroy the immature stages of these insects. Thanasimus dubius is one of the most important predators of destructive bark beetles in the Eastern United States. The adult is 7 to 10 mm long with the head, thorax, and base of the wing covers being a dull red. The antennae and legs are red to black, and the wing covers are mostly black with crossbands of whitish hairs. The larva is elongate, spindle-shaped, and purplish with several dark brown hardened areas on the body. Winter is spent in the larval, pupal, or adult stages. In early spring, the adults emerge and fly to bark beetle-infested trees or logs and feed on the adult prey as they emerge from hibernation. Eggs are deposited in entrances to bark beetle galleries. Young checkered beetle larvae feed on bark beetle eggs; older ones feed on host larvae, pupae, and adults. Pupation occurs in cells in the outer bark. checkered beetle Thanasimus dubius (Fabricius) Checkered beetles in the family Cleridae are among the most important insect predators attacking forest insect pests. Adults of most species are active, antlike, brightly colored, hairy beetles that prey on adult beetles.
    [Show full text]
  • Intégration De La Caractérisation De La Sévérité Du Feu Dans Les Outils D’Aménagement Écosystémique En Forêt Boréale
    Intégration de la caractérisation de la sévérité du feu dans les outils d’aménagement écosystémique en forêt boréale Thèse Jonathan Boucher Doctorat en Sciences forestières Philosophiae Doctor (Ph.D.) Québec, Canada © Jonathan Boucher, 2016 Intégration de la caractérisation de la sévérité du feu dans les outils d’aménagement écosystémique en forêt boréale Thèse Jonathan Boucher Sous la direction de : Éric Bauce, directeur de recherche Christian Hébert, codirecteur de recherche Résumé Chaque année en forêt boréale, les feux génèrent de grandes quantités d’arbres morts au Québec. Considérés comme une perte de revenu potentiel pour l'économie, le gouvernement demande qu'une partie de ces arbres soit récupérée. C'est d'ailleurs une pratique connaissant une tendance à la hausse au niveau mondial. Par contre, la récupération de ce bois est régie par diverses contraintes, dont la rentabilité des opérations et le respect des normes d'aménagement forestier écosystémique (AFE) visant la conservation de la biodiversité associée aux forêts brûlées. La mise en application de l'AFE nécessite de connaître l'impact du feu sur la forêt et ce de façon spatialement explicite. Dans cette optique, nous avons d’abord évalué la sévérité du feu sur le terrain dans 60 sites d’études répartis à travers cinq brûlis. Nous avons ensuite évalué le potentiel du « differenced Normalized Burn Ratio » (dNBR), une méthode de télédétection développée par des chercheurs américains pour estimer la sévérité du feu, à offrir une représentation fidèle des conditions de terrain. Les résultats positifs de cette étape nous ont permis de considérer le dNBR pour bonifier les outils d’aménagement utilisés en forêts brûlées.
    [Show full text]