Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractInfluence of S. cerevisiae and P. kluyveri as starters on chocolate flavour    Next Abstract"Effect of storage time and heat processing on the volatile profile of Senegalese sole (Solea senegalensis Kaup, 1858) muscle" »

J Chem Ecol


Title:"Identification, synthesis, and field testing of the sex pheromone of the citrus leafminer, Phyllocnistis citrella"
Author(s):Moreira JA; McElfresh JS; Millar JG;
Address:"Department of Entomology, University of California, Riverside, CA 92521, USA"
Journal Title:J Chem Ecol
Year:2006
Volume:20060226
Issue:1
Page Number:169 - 194
DOI: 10.1007/s10886-006-9359-6
ISSN/ISBN:0098-0331 (Print) 0098-0331 (Linking)
Abstract:"The citrus leafminer is an important vector of citrus canker in many of the major citrus production areas of the world. (7Z,11Z)-Hexadecadienal was reported as a sex attractant for this insect in the 1980s, based on trap catches during pheromone screening trials in Japan. However, attempts to reproduce this work in other areas of the world have not been successful. We report here that (7Z,11Z)-hexadecadienal is only one component of the pheromone, with the other critical component being the analogous trienal, (7Z,11Z,13E)-hexadecatrienal. Both compounds were identified in the effluvia from live female moths by coupled gas chromatography (GC)-electroantennography using nonpolar and polar GC columns, and the identifications were confirmed by comparisons of mass spectra with those of authentic standards. Stereoisomers of the two compounds, and a number of analogs, were synthesized to confirm the identifications. In field trials, neither compound alone was attractive to male moths, but blends of the two were highly attractive, with thousands of insects being caught per trial. Addition of the isomeric (7Z,11Z,13Z)-hexadecatrienal inhibited attraction to the two-component blend"
Keywords:"Animals Chromatography, Gas Magnetic Resonance Spectroscopy Mass Spectrometry Moths/*chemistry Sex Attractants/chemical synthesis/*chemistry/pharmacology Spectrophotometry, Infrared;"
Notes:"MedlineMoreira, Jardel A McElfresh, J Steven Millar, Jocelyn G eng Research Support, Non-U.S. Gov't 2006/03/10 J Chem Ecol. 2006 Jan; 32(1):169-94. doi: 10.1007/s10886-006-9359-6. Epub 2006 Feb 26"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024