Proposed Program for Management of the Woodwasp Sirex Noctilio Fabricus (Hymenoptera: Siricidae)
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The Ecology, Behavior, and Biological Control Potential of Hymenopteran Parasitoids of Woodwasps (Hymenoptera: Siricidae) in North America
REVIEW:BIOLOGICAL CONTROL-PARASITOIDS &PREDATORS The Ecology, Behavior, and Biological Control Potential of Hymenopteran Parasitoids of Woodwasps (Hymenoptera: Siricidae) in North America 1 DAVID R. COYLE AND KAMAL J. K. GANDHI Daniel B. Warnell School of Forestry and Natural Resources, University of Georgia, Athens, GA 30602 Environ. Entomol. 41(4): 731Ð749 (2012); DOI: http://dx.doi.org/10.1603/EN11280 ABSTRACT Native and exotic siricid wasps (Hymenoptera: Siricidae) can be ecologically and/or economically important woodboring insects in forests worldwide. In particular, Sirex noctilio (F.), a Eurasian species that recently has been introduced to North America, has caused pine tree (Pinus spp.) mortality in its non-native range in the southern hemisphere. Native siricid wasps are known to have a rich complex of hymenopteran parasitoids that may provide some biological control pressure on S. noctilio as it continues to expand its range in North America. We reviewed ecological information about the hymenopteran parasitoids of siricids in North America north of Mexico, including their distribution, life cycle, seasonal phenology, and impacts on native siricid hosts with some potential efÞcacy as biological control agents for S. noctilio. Literature review indicated that in the hymenop- teran families Stephanidae, Ibaliidae, and Ichneumonidae, there are Þve genera and 26 species and subspecies of native parasitoids documented from 16 native siricids reported from 110 tree host species. Among parasitoids that attack the siricid subfamily Siricinae, Ibalia leucospoides ensiger (Norton), Rhyssa persuasoria (L.), and Megarhyssa nortoni (Cresson) were associated with the greatest number of siricid and tree species. These three species, along with R. lineolata (Kirby), are the most widely distributed Siricinae parasitoid species in the eastern and western forests of North America. -
Biology and Ecology of Sirex, Deladenus and Amylostereum in North America
BIOLOGY AND ECOLOGY OF SIREX, DELADENUS AND AMYLOSTEREUM IN NORTH AMERICA A thesis Presented to the Faculty of the Graduate School of Cornell University in Partial Fulfillment of the Requirements for the Degree of Master of Science By Isis Andréia Lima Caetano January, 2017 i © 2017 Isis Andréia Lima Caetano iii Abstract Sirex noctilio is a woodwasp that attacks stressed or dying pine trees. It is native to Eurasia and North Africa but has been invasive in the southern hemisphere since the early 1900s. It was found for the first time in the United States in New York State in September 2004 and in Ontario in 2005. Since then it has spread to a total of seven northeastern US states. S. noctilio is more aggressive than the native pine specialist Sirex nigricornis and it is able to kill living pines by injecting a phytotoxic venom and its symbiotic fungus Amylostereum areolatum into tree trunks. The Kamona strain of the nematode Deladenus siricidicola has been extensively used as a biological control agent against invasive S. noctilio in the Southern Hemisphere, where it sterilizes female hosts by entering the eggs and making them inviable. In North America, a non- sterilizing (NS) strain of D. siricidicola, thought to have been introduced with S. noctilio, is commonly found parasitizing this invasive woodwasp. Species of Deladenus that parasitize Sirex have a parasitic form as well as a mycophagous form. Studies were conducted to understand 1. Sirex mating behavior and sexual receptivity, 2. the growth of two strains of D. siricidicola, Kamona and NS, with different strains and species of Amylostereum spp. -
Putative Source of the Invasive Sirex Noctilio Fungal Symbiont, Amylostereum Areolatum, in the Eastern United States and Its Association with Native Siricid Woodwasps
mycological research 113 (2009) 1242–1253 journal homepage: www.elsevier.com/locate/mycres Putative source of the invasive Sirex noctilio fungal symbiont, Amylostereum areolatum, in the eastern United States and its association with native siricid woodwasps Charlotte NIELSENa, David W. WILLIAMSb, Ann E. HAJEKa,* aDepartment of Entomology, Cornell University, Comstock Hall, Ithaca, NY 14853-2601, USA bUSDA APHIS, PPQ, CPHST, Otis Laboratory, Buzzards Bay, MA 02542, USA article info abstract Article history: Two genotypes of the fungal symbiont Amylostereum areolatum are associated with the Received 16 March 2009 invasive woodwasp Sirex noctilio first found in North America in 2004. S. noctilio is native Received in revised form to Europe but has been introduced to Australasia, South America and Africa where it has 30 July 2009 caused enormous losses in pine plantations. Based on nucleotide sequence data from Accepted 3 August 2009 the intergenic spacer region (IGS) of the nuclear ribosomal DNA, the A. areolatum genotypes Available online 27 August 2009 found in North America are most similar to genotypes found in Europe, and not to Corresponding Editor: Roy E. Halling genotypes from the southern hemisphere. Although two IGS strains of A. areolatum were found in North America it cannot be stated whether A. areolatum was introduced to North Keywords: America from Europe once or twice based on our study. Genetic groupings formed by Fungal symbiont sequencing data were in most cases supported by vegetative compatibility groups Homobasidiomycete (VCGs). Other siricid woodwasp species in the genus Sirex are native to North America. Invasive species The North American native Sirex edwardsii emerging from the same tree as S. -
THE SIRICID WOOD WASPS of CALIFORNIA (Hymenoptera: Symphyta)
Uroce r us californ ic us Nott on, f ema 1e. BULLETIN OF THE CALIFORNIA INSECT SURVEY VOLUME 6, NO. 4 THE SIRICID WOOD WASPS OF CALIFORNIA (Hymenoptera: Symphyta) BY WOODROW W. MIDDLEKAUFF (Department of Entomology and Parasitology, University of California, Berkeley) UNIVERSITY OF CALIFORNIA PRESS BERKELEY AND LOS ANGELES 1960 BULLETIN OF THE CALIFORNIA INSECT SURVEY Editors: E. G: Linsley, S. B. Freeborn, P. D. Hurd, R. L. Usinget Volume 6, No. 4, pp. 59-78, plates 4-5, frontis. Submitted by editors October 14, 1958 Issued April 22, 1960 Price, 50 cents UNIVERSITY OF CALIFORNIA PRESS BERKELEY AND LOS ANGELES CALIFORNIA CAMBRIDGE UNIVERSITY PRESS LONDON, ENGLAND PRINTED BY OFFSET IN THE UNITED STATES OF AMERICA THE SIRICID WOOD WASPS OF CALIFORNIA (Hymenoptera: Symphyta) BY WOODROW W. MIDDLEKAUFF INTRODUCTION carpeting. Their powerful mandibles can even cut through lead sheathing. The siricid wood wasps are fairly large, cylin- These insects are widely disseminated by drical insects; usually 20 mm. or more in shipments of infested lumber or timber, and length with the head, thorax, and abdomen of the adults may not emerge until several years equal width. The antennae are long and fili- have elapsed. Movement of this lumber and form, with 14 to 30 segments. The tegulae are timber tends to complicate an understanding minute. Jn the female the last segment of the of the normal distribution pattern of the spe- abdomen bears a hornlike projection called cies. the cornus (fig. 8), whose configuration is The Nearctic species in the family were useful for taxonomic purposes. This distinc- monographed by Bradley (1913). -
The Sirex Woodwasp, Sirex Noctilio: Pest in North America May Be the Ecology, Potential Impact, and Management in the Southeastern U.S
SREF-FH-003 June 2016 woodwasp has not become a major The Sirex woodwasp, Sirex noctilio: pest in North America may be the Ecology, Potential Impact, and Management in the Southeastern U.S. many insects that are competitors or natural enemies. Some of these insects compete for resources AUTHORED BY: LAUREL J. HAAVIK AND DAVID R. COYLE (e.g. native woodwasps, bark and ambrosia beetles, and longhorned beetles) while others (e.g.parasitoids) are natural enemies and use Sirex woodwasp larvae as hosts. However, should the Sirex woodwasp arrive in the southeastern U.S., with its abundant pine plantations and areas of natural pine, this insect could easily be a major pest for the region. Researchers have monitored and tracked Sirex woodwasp populations since its discovery in North America. The most common detection tool is a flight intercept trap (Fig. 2a) baited with a synthetic chemical lure that consists of pine scents (70% α-pinene, 30% β-pinene) or actual pine branches (Fig. 2b). Woodwasps are attracted to the odors given off by the lure or cut pine branches, and as they fly toward the scent they collide with the sides of the trap and drop Figure 1. The high density of likely or confirmed pine (Pinus spp.) hosts of the Sirex woodwasp suggests the southeastern U.S. may be heavily impacted should this non-native insect become into the collection cup at the bottom. established in this region. The collection cup is usually filled with a liquid (e.g. propylene glycol) that acts as both a killing agent and Overview and Detection preservative that holds the insects until they are collected. -
The New York Forest Owner a Publication of the New York Forest Owners Association for People Who Care About New York’S Trees and Forests May/June 2010
The New York Forest Owner A PublicAtion of the new York forest owners AssociAtion For people who care about New York’s trees and forests May/June 2010 Member Profile: Larry Becker Volume 48 Number 3 www.nyfoa.org The New York In This Issue . ForesT owNers from the President Mike Seager ................................................................................................. 3 AssociATioN whY cAn’t i move firewood? Officers & Directors Justin A. PerrY .......................................................................................... 5 Mike Seager, President PO Box 1281 forest science becomes forest PrActice Pittsford, NY 14535; (585) 414-6511 Peter smAllidge ......................................................................................... 6 Fred Thurnherr, Vice-President 7885 Center Road new York stAte tree fArm news Holland, NY 14080; (716) 941-5736 Erin o’neill ............................................................................................. 8 Rich Taber, Secretary 1703 Fisk Rd kid’s corner Eaton, NY 13334; (315) 837-4265 RebeccA hArgrAve .................................................................................... 9 Mike Birmingham, Treasurer wild things in Your woodlAnds PO Box 601 Kristi sullivAn ........................................................................................... 10 Kinderhook, NY 12106; (518)758-2621 Otis Barber, Sinclairville, (716) 962-8175. 2012 nYfoA sAfetY tiP ..................................................................................... 11 René Germain, -
The Good, the Bad and the Tasty: the Many Roles of Mushrooms
available online at www.studiesinmycology.org STUDIES IN MYCOLOGY 85: 125–157. The good, the bad and the tasty: The many roles of mushrooms K.M.J. de Mattos-Shipley1,2, K.L. Ford1, F. Alberti1,3, A.M. Banks1,4, A.M. Bailey1, and G.D. Foster1* 1School of Biological Sciences, Life Sciences Building, University of Bristol, 24 Tyndall Avenue, Bristol, BS8 1TQ, UK; 2School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK; 3School of Life Sciences and Department of Chemistry, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK; 4School of Biology, Devonshire Building, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK *Correspondence: G.D. Foster, [email protected] Abstract: Fungi are often inconspicuous in nature and this means it is all too easy to overlook their importance. Often referred to as the “Forgotten Kingdom”, fungi are key components of life on this planet. The phylum Basidiomycota, considered to contain the most complex and evolutionarily advanced members of this Kingdom, includes some of the most iconic fungal species such as the gilled mushrooms, puffballs and bracket fungi. Basidiomycetes inhabit a wide range of ecological niches, carrying out vital ecosystem roles, particularly in carbon cycling and as symbiotic partners with a range of other organisms. Specifically in the context of human use, the basidiomycetes are a highly valuable food source and are increasingly medicinally important. In this review, seven main categories, or ‘roles’, for basidiomycetes have been suggested by the authors: as model species, edible species, toxic species, medicinal basidiomycetes, symbionts, decomposers and pathogens, and two species have been chosen as representatives of each category. -
A Review of the Genus Amylostereum and Its Association with Woodwasps
70 South African Journal of Science 99, January/February 2003 Review Article A review of the genus Amylostereum and its association with woodwasps B. Slippers , T.A. Coutinho , B.D. Wingfield and M.J. Wingfield Amylostereum.5–7 Today A. chailletii, A. areolatum and A. laevigatum are known to be symbionts of a variety of woodwasp species.7–9 A fascinating symbiosis exists between the fungi, Amylostereum The relationship between Amylostereum species and wood- chailletii, A. areolatum and A. laevigatum, and various species of wasps is highly evolved and has been shown to be obligatory siricid woodwasps. These intrinsic symbioses and their importance species-specific.7–10 The principal advantage of the relationship to forestry have stimulated much research in the past. The fungi for the fungus is that it is spread and effectively inoculated into have, however, often been confused or misidentified. Similarly, the new wood, during wasp oviposition.11,12 In turn the fungus rots phylogenetic relationships of the Amylostereum species with each and dries the wood, providing a suitable environment, nutrients other, as well as with other Basidiomycetes, have long been unclear. and enzymes that are important for the survival and develop- Recent studies based on molecular data have given new insight ment of the insect larvae (Fig. 1).13–17 into the taxonomy and phylogeny of the genus Amylostereum. The burrowing activity of the siricid larvae and rotting of the Molecular sequence data show that A. areolatum is most distantly wood by Amylostereum species makes this insect–fungus symbio- related to other Amylostereum species. Among the three other sis potentially harmful to host trees, which include important known Amylostereum species, A. -
Re-Thinking the Classification of Corticioid Fungi
mycological research 111 (2007) 1040–1063 journal homepage: www.elsevier.com/locate/mycres Re-thinking the classification of corticioid fungi Karl-Henrik LARSSON Go¨teborg University, Department of Plant and Environmental Sciences, Box 461, SE 405 30 Go¨teborg, Sweden article info abstract Article history: Corticioid fungi are basidiomycetes with effused basidiomata, a smooth, merulioid or Received 30 November 2005 hydnoid hymenophore, and holobasidia. These fungi used to be classified as a single Received in revised form family, Corticiaceae, but molecular phylogenetic analyses have shown that corticioid fungi 29 June 2007 are distributed among all major clades within Agaricomycetes. There is a relative consensus Accepted 7 August 2007 concerning the higher order classification of basidiomycetes down to order. This paper Published online 16 August 2007 presents a phylogenetic classification for corticioid fungi at the family level. Fifty putative Corresponding Editor: families were identified from published phylogenies and preliminary analyses of unpub- Scott LaGreca lished sequence data. A dataset with 178 terminal taxa was compiled and subjected to phy- logenetic analyses using MP and Bayesian inference. From the analyses, 41 strongly Keywords: supported and three unsupported clades were identified. These clades are treated as fam- Agaricomycetes ilies in a Linnean hierarchical classification and each family is briefly described. Three ad- Basidiomycota ditional families not covered by the phylogenetic analyses are also included in the Molecular systematics classification. All accepted corticioid genera are either referred to one of the families or Phylogeny listed as incertae sedis. Taxonomy ª 2007 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Introduction develop a downward-facing basidioma. -
Sequence Data Reflect the Introduction Pathways of the Sirex Woodwasp Parasitoid, Ibalia Leucospoides (Ibaliidae, Hymenoptera)
Sequence data reflect the introduction pathways of the Sirex woodwasp parasitoid, Ibalia leucospoides (Ibaliidae, Hymenoptera) Brett P. Hurley1,*, Katrin N.E. Fitza2, Michael J. Wingfield2, Bernard Slippers2 1Department of Zoology and Entomology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, 0002, South Africa 2Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, 0002, South Africa *Correspondence: Brett P. Hurley. Tel.: +27 12 4205822; fax: +27 12 4203960. e-mail: [email protected] Abstract 1. The parasitoid wasp Ibalia leucospoides is native to the northern hemisphere and has been introduced to the southern hemisphere as a biological control agent for the invasive woodwasp Sirex noctilio. Two sub-species of the parasitoid, I. leucospoides leucospoides (Palearctic distribution) and I. leucospoides ensiger (Nearctic distribution), were introduced and are reported to have hybridized. 2. Despite extensive records of the numbers and origins of the wasps imported into the southern hemisphere, nothing is known regarding their current population diversity. We investigated the genetic variation of I. leucospoides in its native and introduced ranges using mitochondrial (COI) and nuclear (ITS) markers. 3. Mitochondrial DNA diversity in the introduced range was limited, with only five haplotypes, but sequence divergence between these haplotypes was high. Similarly, the ITS rDNA sequences revealed multiple clades present in the introduced range. 4. These results reflect introductions from a wide geographical range, but where genetic bottlenecks have possibly reduced the genetic diversity. The data further reflect the origin of the I. leucospoides populations in South America and South Africa from New Zealand or Australia. -
Minnesota's Top 124 Terrestrial Invasive Plants and Pests
Photo by RichardhdWebbWebb 0LQQHVRWD V7RS 7HUUHVWULDO,QYDVLYH 3ODQWVDQG3HVWV 3ULRULWLHVIRU5HVHDUFK Sciencebased solutions to protect Minnesota’s prairies, forests, wetlands, and agricultural resources Contents I. Introduction .................................................................................................................................. 1 II. Prioritization Panel members ....................................................................................................... 4 III. Seventeen criteria, and their relative importance, to assess the threat a terrestrial invasive species poses to Minnesota ...................................................................................................................... 5 IV. Prioritized list of terrestrial invasive insects ................................................................................. 6 V. Prioritized list of terrestrial invasive plant pathogens .................................................................. 7 VI. Prioritized list of plants (weeds) ................................................................................................... 8 VII. Terrestrial invasive insects (alphabetically by common name): criteria ratings to determine threat to Minnesota. .................................................................................................................................... 9 VIII. Terrestrial invasive pathogens (alphabetically by disease among bacteria, fungi, nematodes, oomycetes, parasitic plants, and viruses): criteria ratings -
United States Department of Agriculture Forest Service Alaska
United States Department of Agriculture Forest Service Alaska Region State and Private Forestry Forest Health Protection 2009 Cover photos clockwise from top: Spruce bark beetle damage (inset spruce bark beetle) Chicken of the woods conks Hemlock fluting and wood decay Wood wasp 2 Insects and Diseases of Alaskan Forests Edward Holsten, U.S. Forest Service Entomologist (retired) Paul Hennon, U.S. Forest Service Pathologist Lori Trummer, U.S. Forest Service Pathologist James Kruse, U.S. Forest Service Entomologist Mark Schultz, U.S. Forest Service Entomologist John Lundquist, U.S. Forest Service Entomologist Publication Number R10–TP–140 3 Acknowledgments The authors thank Tom Laurent, Richard Werner, and John Hard, retired U.S. Forest Service Pathologist and Entomologists, respectively, who were instrumental in developing previous editions of this handbook. We thank Courtney Danley, biological technician, U.S. Forest Service Juneau, for her efforts in obtaining new insect photos. We also appreciate the technical assistance of Ken Zogas, biological technician, U.S. Forest Service Anchorage, and Roger Burnside, Entomologist, Division of Forestry, State of Alaska, as well as the enthusiasm and professionalism of the Alaska Cooperative Extension IPM Technicians. This handbook would not have been possible without the hard work and dedication of David Allen, graphic designer, Public Affairs Office, Chugach National Forest, Anchorage, Alaska. Photographs and other illustrations were obtained, as credited in the Appendix, from individuals and from the files of the State of Alaska, Canadian Forestry Service, the U.S. Forest Service, and other sources as cited. Preface The U.S. Forest Service publication, Identification of Destructive Alaska Forest Insects (91), dealt mainly with the damaging forest insects of Southeastern Alaska.