Identification of a minor component of the sex pheromone of the leopard moth (Zeuzera pyrina L.; Lepidoptera, Cossidae) by capillary gas chromatography

1993 ◽  
Vol 16 (2) ◽  
pp. 123-125 ◽  
Author(s):  
Christian Malosse ◽  
Charles Descoins ◽  
Brigitte Frerot
Author(s):  
Joseph N. Schumacher

AbstractThis study was undertaken to determine if Maryland tobacco contains any unique flavour components and to compare its composition to that of flue-cured and Burley tobaccos. Methylene chloride extracts prepared from these tobaccos were fractionated by liquid-liquid partitions and by preparative liquid chromatography. The resulting fractions were analysed by glass capillary gas chromatography and by glass capillary gas chromatography / mass spectroscopy. The essential oils of these tobaccos were also examined. Only one minor component was found in Maryland tobacco that was not found in the other tobaccos. If the minor and trace components were further studied, other differences might be found. Based on this study, however, the uniqueness of Maryland tobacco is primarily, if not entirely, due to quantitative differences. Also, Maryland tobacco is no more similar to Burley (middle-stalk or low-stalk leaves) than it is to flue-cured tobacco.


2007 ◽  
Vol 34 (1) ◽  
pp. 99-102 ◽  
Author(s):  
Joachim Ruther ◽  
Sven Steiner ◽  
Leif-Alexander Garbe

1980 ◽  
Vol 35 (1-2) ◽  
pp. 45-48 ◽  
Author(s):  
D. L. Struble ◽  
H. Arn ◽  
H. R. Buser ◽  
E. Städler ◽  
J. Freuler

Abstract Evidence obtained by glass capillary gas chromatography coupled to an electroantennographic detector or a mass spectrometer confirmed that Z-11-hexadecenyl acetate is the major component in the pheromone gland washes of calling Mamestra brassicae female moths. Three other components were identified, tetradecanyl acetate, hexadecanyl acetate and E-11-hexadecenyl acetate; but none of these had obvious synergistic effects in attracting males in field tests. The attraction of males to Z -11-hexadecenyl acetate was inhibited by 0.1% Z -11-hexadecenol or 1% Z-9- tetradecenyl acetate.


Chemoecology ◽  
2020 ◽  
Author(s):  
Lea C. Böttinger ◽  
Frederic Hüftlein ◽  
Johannes Stökl

AbstractA major hypothesis for the evolution of chemical signals is that pheromones arise from non-communicative precursor compounds. However, data supporting this hypothesis are rare, primarily because the original functions of the antecedent compounds often have been lost. A notable exception, however, is the parasitoid wasp species Leptopilina heterotoma, whose compound (−)-iridomyrmecin is used as a defensive secretion, a cue for females to avoid competition with con- and hetero-specific females, and as the primary component of the females’ sex pheromone. To better understand the evolution of sex pheromones from defensive compounds, we examined the chemical ecology of L. pacifica, the sister species of L. heterotoma. Here, we show that L. pacifica also produces a defensive secretion containing a species-specific mixture of mostly iridoid compounds. However, the composition of the secretion is more complex than in L. heterotoma, and iridomyrmecin is only a minor component. Moreover, in contrast to L. heterotoma, conspecific female competitors were not avoided by female subjects, and a role of the iridoids in the female sex pheromone of L. pacifica can be excluded, as only the females’ cuticular hydrocarbons (CHCs) resulted in the elicitation of courtship by males. Although closely related, the two sister species show substantial differences in the use of the defensive secretion for communicative purposes. Variation in pheromone usage in this genus still presents a conundrum, highlighting the need for additional studies to understand the selective forces shaping the evolution of pheromone composition.


1990 ◽  
Vol 16 (5) ◽  
pp. 1471-1483 ◽  
Author(s):  
M. Riba ◽  
J. A. Rosell ◽  
M. Eizaguirre ◽  
R. Canela ◽  
A. Guerrero

1986 ◽  
Vol 12 (6) ◽  
pp. 1545-1558 ◽  
Author(s):  
C. Tonini ◽  
G. Cassani ◽  
P. Massardo ◽  
G. Guglielmetti ◽  
P. L. Castellari

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3064 ◽  
Author(s):  
André Marques ◽  
Ana Peixoto ◽  
D. Provance ◽  
Maria Kaplan

The technique of high-speed countercurrent chromatography was applied to the isolation of compounds in essential oil derived from the leaves of Piper mollicomum species. Plant leaves (200.0 g) were submitted to hydrodistillation in a modified Clevenger apparatus. The resulting crude leaf essential oil was analyzed by gas chromatography with flame ionization detector (GC-FID) and gas chromatography-mass spectrometry (GC-MS) to determine the profile of the components. The purified fractions were composed of monoterpenes and sesquiterpenes such as camphor (85.0 mg at 98.5% purity), (E)-nerolidol (100.0 mg at 92.8% purity), and camphene (150.0 mg at 82.0% purity). A minor component of the essential oil, bornyl acetate (16.2 mg at 91.2% purity) was also isolated in the one-step separation protocol in 2 h. The countercurrent chromatography technique proved to be a fast and efficient method for the separation of volatile metabolites that conserved the solvent while delivering various fractions of high purity.


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