Effectiveness of Pheromone Mating Disruption for the Ponderosa
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Section 2. Jack Pine (Pinus Banksiana)
SECTION 2. JACK PINE - 57 Section 2. Jack pine (Pinus banksiana) 1. Taxonomy and use 1.1. Taxonomy The largest genus in the family Pinaceae, Pinus L., which consists of about 110 pine species, occurs naturally through much of the Northern Hemisphere, from the far north to the cooler montane tropics (Peterson, 1980; Richardson, 1998). Two subgenera are usually recognised: hard pines (generally with much resin, wood close-grained, sheath of a leaf fascicle persistent, two fibrovascular bundles per needle — the diploxylon pines); and soft, or white pines (generally little resin, wood coarse-grained, sheath sheds early, one fibrovascular bundle in a needle — the haploxylon pines). These subgenera are called respectively subg. Pinus and subg. Strobus (Little and Critchfield, 1969; Price et al., 1998). Occasionally, one to about half the species (20 spp.) in subg. Strobus are classified instead in a variable subg. Ducampopinus. Jack pine (Pinus banksiana Lamb.) and its close relative lodgepole pine (Pinus contorta Dougl. Ex Loud.) are in subg. Pinus, subsection Contortae, which is classified either in section Trifoliis or a larger section Pinus (Little and Critchfield, 1969; Price et al., 1998). Additionally, subsect. Contortae usually includes Virginia pine (P. virginiana) and sand pine (P. clausa), which are in southeastern USA. Jack pine has two quite short (2-5 cm) stiff needles per fascicle (cluster) and lopsided (asymmetric) cones that curve toward the branch tip, and the cone scales often have a tiny prickle at each tip (Kral, 1993). Non-taxonomic ecological or biological variants of jack pine have been described, including dwarf, pendulous, and prostrate forms, having variegated needle colouration, and with unusual branching habits (Rudolph and Yeatman, 1982). -
Insects and Diseases
INSECTS AND DISEASES Important Problems of Florida’s Forest and Shade Tree Resources INSECTS AND DISEASES Important Problems of Florida’s Forest and Shade Tree Resources by Edward L. Barnard Pathologist, Florida Division of Forestry and Wayne N. Dixon Entomologist, Florida Division of Forestry Illustrations by Wayne N. Dixon Table of Contents FOREWORD ................................................................................................................... 7 INTRODUCTION ............................................................................................................. 8 ACKNOWLEDGEMENTS ............................................................................................... 9 HOW TO USE THE BOOK ............................................................................................ 10 DAMAGE KEYS ............................................................................................................ 11 Tree Insects – Key 1 Conifer Foliage .......................................................................... 11 Tree Insects – Key 2 Conifer Branch and Stem .......................................................... 1 Tree Insects – Key 3 Hardwood Foliage ...................................................................... 2 Tree Insects – Key 4 Hardwood Branch and Stem....................................................... 3 Tree Insects – Key 5 Roots ........................................................................................... 4 Diseases of Trees – Key 1 Conifer Foliage ................................................................. -
Pheromone-Based Disruption of Eucosma Sonomana and Rhyacionia Zozana (Lepidoptera: Tortricidae) Using Aerially Applied Microencapsulated Pheromone1
361 Pheromone-based disruption of Eucosma sonomana and Rhyacionia zozana (Lepidoptera: Tortricidae) using aerially applied microencapsulated pheromone1 Nancy E. Gillette, John D. Stein, Donald R. Owen, Jeffrey N. Webster, and Sylvia R. Mori Abstract: Two aerial applications of microencapsulated pheromone were conducted on five 20.2 ha plots to disrupt western pine shoot borer (Eucosma sonomana Kearfott) and ponderosa pine tip moth (Rhyacionia zozana (Kearfott); Lepidoptera: Tortricidae) orientation to pheromones and oviposition in ponderosa pine plantations in 2002 and 2004. The first application was made at 29.6 g active ingredient (AI)/ha, and the second at 59.3 g AI/ha. Baited sentinel traps were used to assess disruption of orientation by both moth species toward pheromones, and E. sonomana infes- tation levels were tallied from 2001 to 2004. Treatments disrupted orientation by both species for several weeks, with the first lasting 35 days and the second for 75 days. Both applications reduced infestation by E. sonomana,but the lower application rate provided greater absolute reduction, perhaps because prior infestation levels were higher in 2002 than in 2004. Infestations in treated plots were reduced by two-thirds in both years, suggesting that while increas- ing the application rate may prolong disruption, it may not provide greater proportional efficacy in terms of tree pro- tection. The incidence of infestations even in plots with complete disruption suggests that treatments missed some early emerging females or that mated females immigrated into treated plots; thus operational testing should be timed earlier in the season and should comprise much larger plots. In both years, moths emerged earlier than reported pre- viously, indicating that disruption programs should account for warmer climates in timing of applications. -
Arizona Administrative Code Between the Dates of October 1, 2020 Through December 31, 2020 (Supp
3 A.A.C. 4 Supp. 20-4 December 31, 2020 Title 3 TITLE 3. AGRICULTURE CHAPTER 4. DEPARTMENT OF AGRICULTURE - PLANT SERVICES DIVISION The table of contents on the first page contains quick links to the referenced page numbers in this Chapter. Refer to the notes at the end of a Section to learn about the history of a rule as it was published in the Arizona Administrative Register. Sections, Parts, Exhibits, Tables or Appendices codified in this supplement. The list provided contains quick links to the updated rules. This Chapter contains rule Sections that were filed to be codified in the Arizona Administrative Code between the dates of October 1, 2020 through December 31, 2020 (Supp. 20-4). Table 1. Fee Schedule ......................................................47 Questions about these rules? Contact: Name: Brian McGrew Address: Department of Agriculture 1688 W. Adams St. Phoenix, AZ 85007 Telephone: (602) 542-3228 Fax: (602) 542-1004 E-mail: [email protected] Website: https://agriculture.az.gov/plantsproduce/industrial- hemp-program The release of this Chapter in Supp. 20-4 replaces Supp. 20-3, 1-50 pages Please note that the Chapter you are about to replace may have rules still in effect after the publication date of this supplement. Therefore, all superseded material should be retained in a separate binder and archived for future reference. i PREFACE Under Arizona law, the Department of State, Office of the Secretary of State (Office), accepts state agency rule filings and is the publisher of Arizona rules. The Office of the Secretary of State does not interpret or enforce rules in the Administrative Code. -
Longleaf Pine: an Annotated Bibliography, 1946 Through 1967
U.S. Department of Agriculture Forest Service Research Paper SO-35 longleaf pine: an annotated bibliography, 1946 through 1967 Thomas C. Croker, Jr. SOUTHERN FOREST EXPERIMENT STATION T.C. Nelson, Director FOREST SERVICE U.S. DEPARTMENT OF AGRICULTURE 1968 Croker, Thomas C., Jr. 1968. Longleaf pine: an annotated bibliography, 1946 through 1967. Southern Forest Exp. Sta., New Orleans, Louisiana. 52 pp. (U. S. Dep. Agr. Forest Serv. Res. Pap. SO-35) Lists 665 publications appearing since W. G. Wahlenberg compiled the bibliography for his book, Longleaf Pine. Contents Page Introduction .................................................................................................................................... 1 1. Factors of the environment. Biology........................................................................................ 2 11 Site factors, climate, situation, soil ............................................................................. 2 15 Animal ecology. Game management .......................................................................... 2 16 General botany ............................................................................................................. 2 17 Systematic botany ....................................................................................................... 6 18 Plant ecology................................................................................................................. 7 2. Silviculture............................................................................................................................... -
Taxonomic Groups of Insects, Mites and Spiders
List Supplemental Information Content Taxonomic Groups of Insects, Mites and Spiders Pests of trees and shrubs Class Arachnida, Spiders and mites elm bark beetle, smaller European Scolytus multistriatus Order Acari, Mites and ticks elm bark beetle, native Hylurgopinus rufipes pine bark engraver, Ips pini Family Eriophyidae, Leaf vagrant, gall, erinea, rust, or pine shoot beetle, Tomicus piniperda eriophyid mites ash flower gall mite, Aceria fraxiniflora Order Hemiptera, True bugs, aphids, and scales elm eriophyid mite, Aceria parulmi Family Adelgidae, Pine and spruce aphids eriophyid mites, several species Cooley spruce gall adelgid, Adelges cooleyi hemlock rust mite, Nalepella tsugifoliae Eastern spruce gall adelgid, Adelges abietis maple spindlegall mite, Vasates aceriscrumena hemlock woolly adelgid, Adelges tsugae maple velvet erineum gall, several species pine bark adelgid, Pineus strobi Family Tarsonemidae, Cyclamen and tarsonemid mites Family Aphididae, Aphids cyclamen mite, Phytonemus pallidus balsam twig aphid, Mindarus abietinus Family Tetranychidae, Freeranging, spider mites, honeysuckle witches’ broom aphid, tetranychid mites Hyadaphis tataricae boxwood spider mite, Eurytetranychus buxi white pine aphid, Cinara strobi clover mite, Bryobia praetiosa woolly alder aphid, Paraprociphilus tessellatus European red mite, Panonychus ulmi woolly apple aphid, Eriosoma lanigerum honeylocust spider mite, Eotetranychus multidigituli Family Cercopidae, Froghoppers or spittlebugs spruce spider mite, Oligonychus ununguis spittlebugs, several -
Genetic Variation in Resistance of Scotch Pine to Zimmerman Pine Moth
The Great Lakes Entomologist Volume 8 Number 4 - Winter 1975 Number 4 - Winter Article 8 1975 December 1975 Genetic Variation in Resistance of Scotch Pine to Zimmerman Pine Moth Jonathan W. Wright Louis F. Wilson USDA Forest Service John N. Bright Michigan State University Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Wright, Jonathan W.; Wilson, Louis F.; and Bright, John N. 1975. "Genetic Variation in Resistance of Scotch Pine to Zimmerman Pine Moth," The Great Lakes Entomologist, vol 8 (4) Available at: https://scholar.valpo.edu/tgle/vol8/iss4/8 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Wright et al.: Genetic Variation in Resistance of Scotch Pine to Zimmerman Pine THE GREAT LAKES ENTOMOLOGIST GENETIC VARIATION IN RESISTANCE OF SCOTCH PlNE TO ZIMMERMAN PlNE MOTH1 Jonathan W. Wright, Louis F. Wilson and John N. ~ri~ht~ Scotch pine (Pinus sylvestris L.), a forest tree introduced from Eurasia, is commonly planted for Christmas tree and timber use in northeastern United States. In this country it has numerous insect enemies. Among the most important are European pine shoot moth, Rhyacionia buoliana (Schiffermiieller); pine root collar weevil, Hylobius radicis Buchanan;,European pine sawfly, Neodiprion sertifer (Geoffroy); and eastern white-pine shoot borer, Eucosma gloriola Heinrich. Previous studies (Wright et al., 1967; Wright and Wilson, 1972; Steiner, 1974) have revealed large genetic differences in resistance to some of these pests. -
Impacts of Native and Non-Native Plants on Urban Insect Communities: Are Native Plants Better Than Non-Natives?
Impacts of Native and Non-native plants on Urban Insect Communities: Are Native Plants Better than Non-natives? by Carl Scott Clem A thesis submitted to the Graduate Faculty of Auburn University in partial fulfillment of the requirements for the Degree of Master of Science Auburn, Alabama December 12, 2015 Key Words: native plants, non-native plants, caterpillars, natural enemies, associational interactions, congeneric plants Copyright 2015 by Carl Scott Clem Approved by David Held, Chair, Associate Professor: Department of Entomology and Plant Pathology Charles Ray, Research Fellow: Department of Entomology and Plant Pathology Debbie Folkerts, Assistant Professor: Department of Biological Sciences Robert Boyd, Professor: Department of Biological Sciences Abstract With continued suburban expansion in the southeastern United States, it is increasingly important to understand urbanization and its impacts on sustainability and natural ecosystems. Expansion of suburbia is often coupled with replacement of native plants by alien ornamental plants such as crepe myrtle, Bradford pear, and Japanese maple. Two projects were conducted for this thesis. The purpose of the first project (Chapter 2) was to conduct an analysis of existing larval Lepidoptera and Symphyta hostplant records in the southeastern United States, comparing their species richness on common native and alien woody plants. We found that, in most cases, native plants support more species of eruciform larvae compared to aliens. Alien congener plant species (those in the same genus as native species) supported more species of larvae than alien, non-congeners. Most of the larvae that feed on alien plants are generalist species. However, most of the specialist species feeding on alien plants use congeners of native plants, providing evidence of a spillover, or false spillover, effect. -
Pinus Strobus Lm Eastern White Pine Pinaceae Pine Family G
Pinus strobus Lm Eastern White Pine Pinaceae Pine family G. W. Wendel and H. Clay Smith Eastern white pine (Pinus strobus), also called transpiration is between 430 and 710 mm (17 and 28 northern white pine, is one of the most valuable trees in), of which 56 to 68 percent occurs in the warm in eastern North America. Before the arrival of white season. There is a moisture surplus in all seasons. men, virgin stands contained an estimated 3.4 billion Average depth of frost penetration ranges from m3 (600 billion fbm) of lumber. By the late 1800’s about 25 cm (10 in) in the southern Appalachians to most of those vast stands had been logged. Because more than 178 cm (70 in) in parts of central and it is among the more rapid growing northern forest northern Minnesota. Average annual snowfall ranges conifers, it is an excellent tree for reforestation from 13 cm (5 in) in northern Georgia to more than projects, landscaping, and Christmas trees and has 254 cm (100 in) in New England and southern the distinction of having been one of the more widely Canada (51). planted American trees. Soils and Topography Habitat The major soil orders found in the white pine Native Range range are Inceptisols, Ultisols, Spodosols, Entisols, and Alfisols (14,50,66). In New England the impor- Eastern white pine (fig. 1) is found across southern tant subgroups are excessively drained or somewhat Canada from Newfoundland, Anticosti Island, and excessively drained sandy deposits or stratified sand Gasp6 peninsula of Quebec; west to central and and gravel deposits. -
Sirex Science Advisory Panel Report January 9 & 10, 2006
Sirex Science Advisory Panel Report January 9 & 10, 2006 Annapolis, MD 1 Members Robin Bedding – CSIRO Australia Dave Lance – USDA-APHIS-PPQ Angus Carnegie – NSW DPI, Australia Vic Mastro (chair) – USDA-APHIS-PPQ Peter de Groot, CFS Richard Reardon – USDA-FS Kevin Dodds – USDA-FS-FHP Don Rogers – NC Div. of Forest Resources Rene Germain - SUNY-ESF Nathan Schiff – USDA-FS Fred Hain – NC State Jim Tumlinson – Penn State Dennis Haugen – USDA-FS-FHP Dave Williams – USDA-APHIS-PPQ Edson T. Iede, Embrapa Florestas, Brazil 1 See Appendix 2 for C.V.s of SAP members Sirex Science Advisory Panel 10 January, 2006 Panel Recommendations to Sirex Management Team A Sirex noctilio female was found in a trap placed for exotic bark beetle in Fulton, NJ on September 7 of 2004 and identified in February of 2005. Since that time, through visual and trap-based surveys, an established population has been found in the area around Oswego and Fulton, NY. Trap catches indicate that the population may extend at least 46 miles southeast of Oswego. A total of 85 females were captured in NY. In addition, trap surveys in Canada, along the north shore of Lake Ontario and the St. Lawrence River, captured five additional females. One of these was captured as far east as the town of Prescott (Proviena). Sirex noctilio is native to EurAsian and only has become a primary pest of Pinus species when it was accidentally introduced into areas where pines are being commercially grown. It is now known to occur in New Zealand, Australia, South Africa, Brazil, Chili, and Argentina. -
Pine Shoot Borer
www.arborlawn.com 1-800-331-1746 At ArborLawn, one of our primary goals is to further the knowledge of our customers. This information will give you a better understanding of the needs of your trees so you will be able to make more informed decisions regarding their care. PINE SHOOT BORER European Pine Shoot Moth European pine shoot moth (Rhyacionia buoliana) is an important pest of pines. It was originally imported on nursery stock from central Europe around 1914. The moth moved westward from Long Island, New York and by early 1950s it was widespread in North America. Damage is done by larvae that bore in shoot and bud tissue. Attacks frequently occur in young trees. Killed terminals cause bushy growth that may render nursery plants unmarketable or landscape plants unattractive. All pines are attacked but two-needle pines such as lodgepole, mugo, and Scotch pine appear to be especially susceptible. Pines also may differ in their ability to recover from damage by this insect. Adults emerge in early summer. The exact date depends on spring temperatures. Warm spring temperatures permit an earlier emergence whereas a relatively cool spring delays the emergence flight. Female moths lay eggs on host pines that may be scattered over a large area. In other words, EPSM is a relatively strong flier and can therefore effectively disperse its eggs. Eggs hatch in one to two weeks at which time the new larvae begin feeding. Needles are mined first, and then buds. Larvae spend the winter under a resin/silk shelter or in buds. The following spring, larvae migrate upward and feed on new buds or expanding shoots. -
Seed Source-Related Eastern Pineshoot Borer Incidence in Jack Pine
Seed source-related eastern pineshoot borer incidence in jack pine Plant Geneticist North Central Forest Experiment Station USDA Forest Service Institute of Forest Genetics Rhinelander, Wisconsin (Received October / November 1978) Summary Life History Variation among 90 ja& pine seed sources in incidence of BUTCHER and HODSON(1949), D~ooz(1960), and WILSON eastern pineshmt borer was evaluated in 1966 (age 5) in a (1972) have described the life history of the eastern pine- short-term nursery test and yearly from 1970 to 1973 (age shoot borer. Adults elmerge sooin after shoot elongation be- 9-12) in a field test in northern Wiscmsin. There were gins in late April to mid-May, depending on lucality. After cignificant differences among sources in shoot borer inci- mating, the female usually deposits a single egg oa a needle dence at all ages. sheath on each of several new shoots. Within 2 weeks the The results frolm this study show that eastern pineshoot larva emerges and bores into the shoot behind a needle borer incidence in jack pine is under strong genetic control. fascicle, or occasionally behind a coae or bark scale along Variation among sources in borer incidence was signi- the shmt. The larva mines downward in the pith to a point ficantly correlated with variation in total height. But co- 1 to 3 inches above the base uf the current year's shoot. variance analysis showed that variatiun in borer incidence Usually by mid-June the larva reverses direction in the could not be entirely attributed to differences among shoolt and begins to mine upward.