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 AbstractBiogenic ammonia modifies antibiotic resistance at a distance in physically separated bacteria    Next AbstractAnalysis of human skin emanations by gas chromatography/mass spectrometry. 2. Identification of volatile compounds that are candidate attractants for the yellow fever mosquito (Aedes aegypti) »

J Am Soc Mass Spectrom


Title:Gas chromatography/mass spectrometry analysis of the cuticular hydrocarbons from parasitic wasps of the genus Muscidifurax
Author(s):Bernier UR; Carlson DA; Geden CJ;
Address:"USDA-ARS-CMAVE, 1600 SW 23rd Drive, 32608, Gainesville, FL. ubernier@gainesville.usda.ufl.edu. USDA-ARS-CMAVE, 1600 SW 23rd Drive, 32608, Gainesville, FL"
Journal Title:J Am Soc Mass Spectrom
Year:1998
Volume:9
Issue:4
Page Number:320 - 332
DOI: 10.1016/S1044-0305(97)00288-2
ISSN/ISBN:1044-0305 (Print) 1044-0305 (Linking)
Abstract:"Parasitic Hymenoptera can be difficult to identify by conventional taxonomic techniques. Examination of the cuticular hydrocarbons (CHCs) provides a basis for chemotaxonomic differentiation, which may lead to the discovery of pheromones, and can be a means of examining colonies for species cross-contamination. The parasitic wasps examined were Muscidifurax raptor, M. zaraptor, M. uniraptor, and the gregarious form of M. raptorellus. Species within the genus Muscidifurax, as well as the sex, can clearly be differentiated by examining the gas chromatograms of the CHCs. Identification of the alkanes by mass spectrometry shows uncommon dimethylalkanes and trimethylalkanes for members of the genus. The methyl branched cuticular hydrocarbons of these insects are rare compared to those found on insects reported in the literature, but are present in significant amounts on these insects. Additionally, sexual dimorphism is observed in long chain alkanes (C21-C39) present on male and female cuticular surfaces for these species. Females tend to have cuticular hydrocarbons with methyl branches located externally on the carbon backbone chain for dimethyl-, trimethyl-, and tetramethylalkanes, whereas males tend to have dimethyl- and trimethylalkanes located internally on the hydrocarbon backbone chains. Mass spectra of novel and rare methyl branched compounds identified on these parasitoids are presented"
Keywords:
Notes:"PubMed-not-MEDLINEBernier, U R Carlson, D A Geden, C J eng 1998/04/01 J Am Soc Mass Spectrom. 1998 Apr; 9(4):320-32. doi: 10.1016/S1044-0305(97)00288-2"

 
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 24-11-2024