Insektizide · Bakterizide · Oomyceten-Fungizide / Biochemische und biologische Methoden · Naturstoffe / Insecticides · Bactericides · Oomycete Fungicides / Biochemical and Biological Methods · Natural Products von Richard Wegler | ISBN 9783540103073

Insektizide · Bakterizide · Oomyceten-Fungizide / Biochemische und biologische Methoden · Naturstoffe / Insecticides · Bactericides · Oomycete Fungicides / Biochemical and Biological Methods · Natural Products

von Richard Wegler
Buchcover Insektizide · Bakterizide · Oomyceten-Fungizide / Biochemische und biologische Methoden · Naturstoffe / Insecticides · Bactericides · Oomycete Fungicides / Biochemical and Biological Methods · Natural Products | Richard Wegler | EAN 9783540103073 | ISBN 3-540-10307-4 | ISBN 978-3-540-10307-3

Insektizide · Bakterizide · Oomyceten-Fungizide / Biochemische und biologische Methoden · Naturstoffe / Insecticides · Bactericides · Oomycete Fungicides / Biochemical and Biological Methods · Natural Products

von Richard Wegler

Inhaltsverzeichnis

  • Biology of Pheromones.
  • 1. Introduction.
  • 2. Biological Function.
  • 2.1. Sex Pheromones.
  • 2.2. Aggregation Pheromones.
  • 2.3. Inhibitors.
  • 2.4. Allelochemicals.
  • 2.5. Communication Systems.
  • 3. Biosynthesis and Release.
  • 3.1. Stimulation of Production.
  • 3.2. Rhythm of Release.
  • 4. Bioassay Methods.
  • 4.1. Laboratory Bioassays.
  • 4.2. Electrophysiology.
  • 4.3. Field Bioassays.
  • 5. Genetic Factors.
  • 5.1. Alternative Systems.
  • 5.2. Population Variations.
  • 5.3. Taxonomy.
  • 6. Case Histories.
  • 6.1. Dendroctonus frontalis.
  • 6.2. Trypodendron ( = Xyloterus) lineatum.
  • 6.3. Ips typographus.
  • 6.4. Lymantria ( = Porthetria).
  • 7. Conclusions.
  • 8. References.
  • Chemistry of Insect Pheromones.
  • 1. Insect Behavior Controlling Chemicals in Plant Protection.
  • 2. The Chemical Structure of Pheromones.
  • Chemical Structure, Occurence, and Behavioral Release of Insect Pheromones and Pheromone Analogs.
  • 2.1. Sex Attractants of Female Butterflies and Moths, and Related Compounds.
  • 2.2. Pheromones of Male Lepidoptera.
  • 2.3. Pheromones of the Bark Beetles (Scolytidae).
  • 2.4. Sex and Aggregation Pheromones of Other Beetle Families.
  • 2.5. Sex and Aggregation Pheromones of Cockroaches (Blattidae, Orthoptera).
  • 2.6. Alarm Substances of Ants (Formicidae, Hymenoptera).
  • 2.7. Trail Pheromones of Ants and Termites (Formicidae and Isoptera).
  • 2.8. Sex Attractants of Flies (Diptera).
  • 2.9. Aphids and Scales (Homoptera).
  • 2.10. True Bugs (Heteroptera).
  • 2.11. Bees, Wasps, Bumble Bees, Sawflies (Hymenoptera).
  • 3. Physiological and Behavioral Activity of Pheromones.
  • 3.1. Electrophysiology.
  • 3.2. Structure-Activity Relationships.
  • 3.3. Multicomponent Pheromone Complexes.
  • 3.4. Olfactometer Experiments and Field Tests.
  • 4. Isolation and Structure Elucidation of Pheromones.
  • 4.1. General.
  • 4.2. The Bioassay.
  • 4.3. Pheromone Screening.
  • 4.4. Pheromone Sources.
  • 4.5. Isolation of Pheromones.
  • 4.6. Chromatographic Purification and Fractionation for the Identification of Pheromones.
  • a) Gel Permeation Chromatography (GPC).
  • b) Liquid Chromatography under Normal Pressure.
  • c) High Performance Liquid Chromatography (HPLC).
  • d) Thin Layer Chromatography (TLC).
  • e) Gas Chromatography.
  • 4.7. Identification and Structure Elucidation.
  • a) Ultrared Spectroscopy.
  • b) Ultraviolet Spectroscopy.
  • c) Nuclear Magnetic Resonance — NMR — Spectroscopy.
  • d) Mass Spectroscopy.
  • e) Gas Chromatographic Techniques.
  • 5. Synthesis of Insect Pheromones.
  • 5.1. Butterflies and Moths — Lepidoptera.
  • a) Wittig Olefination and Related Methods.
  • b) The “Acetylenic Approach” to Pheromone Synthesis.
  • c) Reduction of Allyl Diethyl Phosphonates.
  • d) Coupling Reactions with Organometallic Reagents.
  • e) [3.3]-Sigmatropic Reactions.
  • f) Transition Metal Catalyzed Metathesis Reaction.
  • g) Electrochemical Procedures.
  • h) Stereoselective Syntheses of Chiral Lepidoptera Pheromones.
  • 5.2. Beetles — Coleoptera.
  • a) Scolytidae — Bark Beetles.
  • b) Dermestidae.
  • c) Curculionidae.
  • d) Bruchidae.
  • 5.3. Flies — Diptera.
  • 5.4. Hymenoptera.
  • 5.5. Pheromones of Isoptera.
  • 5.6. Synthesis of Cockroach Pheromones (Blattaria).
  • 6. Acknowledgement.
  • 7. References.
  • Die praktische Verwendung von Insektenpheromonen.
  • 1. Einleitung.
  • 2. Sexuallockstoffe und Aggregationspheromone.
  • 2.1 Pheromone als Indikatoren.
  • 2.2. Bekämpfung von Schädlingen im Anlockverfahren.
  • 2.3. Störung der chemischen Kommunikation.
  • 2.4. Lockstoffe als Hilfsmittel für andere Verfahren.
  • 3. Anwendungsmöglichkeiten sonstiger Pheromone.
  • 4. Umweltprobleme und Nebenwirkungen.
  • 5. Entwicklung und Stand der Pheromon-Anwendung.
  • 5.1. Forst und Gehölze.
  • 5.2. Obst, Wein, Oliven.
  • 5.3. Getreide.
  • 5.4. Baumwolle.
  • 5.5. Sonstiger Acker- und Gartenbau.
  • 5.6. Vorratsschutz.
  • 5.7. Hygiene, Medizin and Veterinärmedizin.
  • 6. Tendenzen, Probleme, Aussichten und Grenzen.
  • 7. Literatur.
  • The Use of Juvenoids in Insect Pest Management.
  • 2. The Role of Endogenous Juvenile Hormones.
  • 3. Effects of Exogenous Application of Juvenoids.
  • 3.1. Morphogenetic Effects.
  • 3.2. Ovicidal Effects and Disruption of Embryogenesis.
  • 3.3. Effects on the Reproductive System and Fecundity.
  • 3.4. Effects on Diapause, Polymorphism, and Behaviour.
  • 4. The Use of Juvenoids Against Pest Species.
  • 4.1. Pests of Field Crops, Silviculture, and Horticulture.
  • 4.2. Pests of Medical and Veterinary Importance.
  • 4.3. Pests of Stored Products.
  • 4.4. Household, Domestic, and Other Pests.
  • 4.5. The Use of Juvenoids in Sericulture.
  • 5. Some Factors Influencing the Practical Use of Juvenoids.
  • 5.1. Choice of Target Species.
  • 5.2. Metabolism, Resistance, and Synergism.
  • 6. Conclusions.
  • Pflanzenschutzpräparate mikrobieller Herkunft.
  • 1. Einführung.
  • 2. Fungizide und Bakterizide.
  • 2.1. Einleitung.
  • 2.2. Handelsprodukte.
  • 2.3. Forschungs- und Entwicklungspräparate.
  • 3. Insektizide.
  • 3.1. Einleitung.
  • 3.2. Handelsprodukte.
  • 3.3. Forschungs- und Entwicklungspräparate.
  • 4. Herbizide und Wachstumsregulatoren.
  • 4.1. Einleitung.
  • 4.2. Forschungs- und Entwicklungspräparate.
  • Insektizide Phosphorsäureester.
  • 2. Insektizide vom Typ der (Thio)Phosphorsäure-arylester.
  • 3. Insektizide vom Typ der (Thio)Phosphorsäure-heteroarylester.
  • 4. Insektizide vom Typ der (Thio)Phosphorsäure-thioalkylester.
  • 5. Insektizide vom Typ der Enol(thio)phosphorsäureester.
  • 6. Sonstige.
  • Bacterial Plant Diseases and Their Control.
  • 2. The Economic Importance of Bacterioses.
  • 3. The Causative Agents of Bacterioses.
  • 3.1. Classification and Taxonomy.
  • 3.2. Bacterial Genera to which Causative Agents of Bacterioses are Assigned.
  • 4. Examples of Bacterial Plant Diseases.
  • 4.1. Bacterial Leaf Blight of Rice.
  • 4.2. Fire Blight of Pear and Apple.
  • 4.3. Lethal Yellowing of Coconut Palms.
  • 5. Control of Bacterial Plant Diseases.
  • 5.1. Biological Aspects.
  • 5.2. Chemical Control — General Considerations.
  • 6. Chemistry of Bactericidal Compounds.
  • 6.1. Inorganic, Nonmetallic Compounds.
  • 6.2. Inorganic and Organic Metal Compounds.
  • 6.2.1. Mercury Compounds.
  • 6.2.2. Copper Compounds.
  • 6.3. Dithiocarbonates and Dithiocarbamates.
  • 6.4. Alcohols and Other Aliphatic Compounds.
  • 6.5. Aromatic Compounds.
  • 6.6. Heterocyclic Compounds.
  • 6.6.1. Heterocyclics Containing Nitrogen.
  • 6.6.2. Heterocyclics Containing Nitrogen and Sulfur.
  • 6.7. Antibiotics.
  • Recent Advances in the Chemical Control of Oomycetes.
  • 2. Biology of Plant-Pathogenic Oomycetes.
  • 2.1. Foliar Plant Diseases Caused by Oomycetes.
  • 2.2. Soilborne Seedling and Root Diseases Caused by Oomycetes.
  • 3. Traditional Control of Oomycetes by Nonsystemic Fungicides.
  • 4. Chemistry and Biological Properties of Systemic and Specific Fungicides Against Oomycetes.
  • 4.1. Earlier Fungicides with Specific Activity Against Oomycetes.
  • 4.1.1. Fenaminosulf.
  • 4.1.2. Etridiazole.
  • 4.1.3. Chloroneb.
  • 4.1.4. Hymexazol and Related Compounds.
  • 4.2. Pyroxychlor and Other Pyridines.
  • 4.3. Prothiocarb and Propamocarb.
  • 4.4. Curzate.
  • 4.5. Ethyl Phosphites.
  • 4.6. Acylalanines and Related Compounds.
  • 4.7. Miscellaneous New Fungicides Against Oomycetes.
  • 5. Discussion of Disease Control Strategies with the New Systemic Fungicides Against Oomycetes.
  • 5.1. Novel Disease Control Possibilities with Systemic Fungicides.
  • 5.2. Utilization of Curative and Systemic Properties for Integrated Disease Control Strategies.
  • 5.3. The Risk of Fungicide Resistance.
  • 6. References.
  • Benzoylphenylurea Insecticides.
  • 2. Synthesis of 1-benzoyl-3-phenylureas.
  • 3. Diflubenzuron, Physical/Chemical Properties and Analysis.
  • 3.1. Physical and Chemical Properties.
  • 3.2. Analysis.
  • 4. Formulations.
  • 5. Toxicology.
  • 5.1. Mammalian Toxicity.
  • 5.1.1. Acute Toxicity.
  • 5.1.2. Sub-acute Toxicity.
  • 5.1.3. Semi-chronic Toxicity.
  • 5.1.4. Chronic Toxicity.
  • 5.1.5. Special Studies.
  • 5.2. Toxicity to Birds.
  • 5.3 Toxicity to Fish.
  • 6. Mode of Action.
  • 6.1. Biological Aspects.
  • 6.1.1. Larvicidal Effects.
  • 6.1.2. Ovicidal Effects.
  • 6.1.3. Effects on Adult Insects.
  • 6.2. Biochemical Aspects.
  • 7. Distribution and Metabolism.
  • 7.1. Distribution and Degradation of Diflubenzuron in Soil and Water.
  • 7.2. Plants and Other Organic Matrices.
  • 7.3. Animal Metabolism.
  • 7.4. Metabolism in Insects.
  • 7.5. Behaviour in Ecosystems.
  • 7.6. Residues.
  • 7.6.1. Plant Residues.
  • 7.6.2. Residues in Animal Tissues.
  • 7.6.3. Residues in Mushrooms.
  • 8. Fields of Application.
  • 8.1. Introduction; Selectivity.
  • 8.2. Agricultural Crops.
  • 8.2.1. Cotton.
  • 8.2.2. Soybeans.
  • 8.2.3. Corn.
  • 8.3. Horticultural Crops.
  • 8.3.1. Fruit Crops.
  • 8.3.2. Mushrooms.
  • 8.3.3. Floriculture.
  • 8.3.4. Cabbage.
  • 8.4. Forestry and Woody Ornamentals.
  • 8.5. Medical-hygienic and Veterinary Applications, Including Control of Nuisance Insects.
  • 8.5.1. Mosquitoes and Midges.
  • 8.5.2. Flies.
  • 8.5.3. Blackflies.
  • 8.5.4. Tsetse Flies.
  • 8.5.5. Chewing Lice.
  • 8.6. Effects on Non-targets, not Related to a Specific Field of Application.
  • 8.6.1. Honey Bees.
  • 8.6.2. Non-target Aquatic Organisms.
  • 8.7. Nematicidal Effects.
  • 9. Resistance.
  • 9.1. Cross Resistance.
  • 9.2. Build-up of Resistance Against Diflubenzuron.
  • 10. Structure-Activity Relationship.
  • 11. Experimental Products.
  • 11.1. Experimental Compounds of Bayer AG.
  • 11.2. Experimental Compounds of Eli Lilly.
  • 11.3. Experimental Compound of Philips-Duphar.
  • 12. Literature and Patents.
  • Zur Problematik des biologischen Pflanzenschutzes in der Landwirtschaft.
  • 1. Problemstellung und Abgrenzung.
  • 2. Problemumfang.
  • 3. Praktische Aussichten der biologischen Unkrautbekämpfung.
  • 4. Praktische Aussichten der biologischen Bekämpfung von Schadpilzen.
  • 5. Biologische Bekämpfung von Insekten und anderen tierischen Schädlingen.
  • 5.1. Verschleppte Schädlinge.
  • 5.2. Autochthone Schädlinge.
  • 5.3. Methoden der biologischen Schädlingsbekämpfung.
  • 5.3.1. Die Verwendung von Parasiten.
  • 5.3.2. Die Verwendung von Prädatoren.
  • 5.3.3. Die Verwendung von Mikroorganismen.
  • 5.3.4. Autozidverfahren.
  • 6. Nebenwirkungen und Gesichtspunkte der amtlichen Zulassung.
  • 7. Diskussion.
  • 8. Schlußbetrachtung.
  • 9. Literatur.