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« Previous Abstract"Chirality of israeli pine bast scale,Matsucoccus josephi (homoptera: Matsucoccidae) sex pheromone"    Next Abstract"The decoupled direct method for sensitivity analysis in a three-dimensional air quality model--implementation, accuracy, and efficiency" »

Bioorg Med Chem


Title:Antennal response and field attraction of the predator Elatophilus hebraicus (Hemiptera: Anthocoridae) to sex pheromones and analogues of three Matsucoccus spp. (Homoptera: Matsucoccidae)
Author(s):Dunkelblum E; Mendel Z; Gries G; Gries R; Zegelman L; Hassner A; Mori K;
Address:"Institute of Plant Protection, ARO, The Volcani Center, Bet Dagan, Israel"
Journal Title:Bioorg Med Chem
Year:1996
Volume:4
Issue:3
Page Number:489 - 494
DOI: 10.1016/0968-0896(96)00030-2
ISSN/ISBN:0968-0896 (Print) 0968-0896 (Linking)
Abstract:"The predator Elatophilus hebraicus is closely associated with its prey, the pine bast scale, Matsucoccus josephi, and utilizes the M. josephi sex pheromone as a kairomone. Kairomonal activity of E. hebraicus was studied by GC-EAD and field bioassays. The sex pheromone of M. josephi [2E,5R,6E,8E)-5,7-dimethyl-2,6,8-decatrien-4-one [(R)-E-M.j.] elicited a strong EAD response and attracted large numbers of the predator. The sex pheromone of two allopatric Matsucoccus spp., Matsucoccus feytaudi, (3S,7R,8E,10E)-3,7,9-trimethyl-8,10-dodecadien-6-one [(S,R)-E-M.f.] and Matcucossus matsumurae, (2E, 4E,6R,10R)-4,6,10,12-tetramethyl-2,4-tridecadien-7-one [(R,R)-E-M.m.], were also EAD-active and attracted significant numbers of E. hebraicus in the forest. Increasing the lure load of (S,R)-E-M.f. and (R,R)-E-M.m., in order to compensate for their lower volatility relative to (R)-E-M.j., resulted in similar attraction of E. hebraicus to each of the three pheromones. Other Matsucoccus pheromone stereoisomers displayed no behavioral activity. There was a significant difference in the activity of sex pheromone analogues, (6E/Z,8E)-5,7-dimethyl-6,8-decadien-4-one (52% E + 48% Z, ANLG 1) and (6E/Z,8E)-2,4,6-trimethyl- 1,6,8-nonatrien-3-one (60% E + 40% Z, ANLG 2). The (E) isomer of ANLG 1 evoked a strong EAD response from E. hebraicus and the mixture of E/Z ANLG 1 attracted the predator in moderate numbers, whereas ANLG 2 was inactive both in EAD and field tests. Conversely, M. josephi males were not attracted to M. feytaudi and M. matsumurae pheromones or pheromone analogues. Cross-activity of E. hebraicus to M. feytaudi and M. matsumurae pheromones may be based on structural similarity of the compounds. Alternatively, E. hebraicus may respond specifically to the pheromones of two allopatric Matsucoccus spp. If true, kairomonal attraction of E. hebraicus to these pheromones may have evolved during speciation of Matsucoccidae and may have been preserved despite the allopatry of M. josephi, M feytaudi and matsumurae"
Keywords:"Animals Biological Assay Chromatography, Gas Electrophysiology Hemiptera/*physiology Insecta/*physiology Magnetic Resonance Spectroscopy Molecular Conformation Molecular Weight Sex Attractants/*pharmacology Sexual Behavior, Animal Species Specificity;"
Notes:"MedlineDunkelblum, E Mendel, Z Gries, G Gries, R Zegelman, L Hassner, A Mori, K eng Research Support, Non-U.S. Gov't England 1996/03/01 Bioorg Med Chem. 1996 Mar; 4(3):489-94. doi: 10.1016/0968-0896(96)00030-2"

 
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