Production and Distribution of Aldehyde and Alcohol Sex Pheromone Components in the Pheromone Gland of Females of the Moth Chloridea virescens

2018 ◽  
Vol 45 (1) ◽  
pp. 9-17 ◽  
Author(s):  
Stephen P. Foster ◽  
Karin G. Anderson
2006 ◽  
Vol 61 (3-4) ◽  
pp. 278-284 ◽  
Author(s):  
Raimondas Mozūraitis ◽  
Vidmantas Karaliusa ◽  
Vincas Būda ◽  
Anna-Karin Borg-Karlson

Gas chromatography and mass spectrometry analyses of crude sex pheromone gland extracts revealed that virgin Synanthedon tipuliformis (Clerck), currant borer (Lepidoptera: Sesiidae) females, produced 6 compounds, structurally related to sex pheromone components of clearwing moths. By comparison of retention times and mass spectra of natural products with corresponding properties of synthetic standards, these compounds were identified as: (2E,13Z)-octadeca-2,13-dien-1-yl acetate (E2,Z13-18:OAc), (3E,13Z)-octadeca-3,13-dien-1-yl acetate (E3,Z13-18:OAc), (13Z)-octadec-13-en-1-yl acetate (Z13-18:OAc), (2E,13Z)-octadeca- 2,13-dien-1-ol (E2,Z13-18:OH), (13Z)-octadec-13-en-1-ol (Z13-18:OH) and octadecan- 1-ol (18:OH) in the ratio 100:0.7:2.7:3.2:traces:traces. The first 3 compounds were previously known to occur in the sex pheromone gland extracts of currant borers, while the last 3 chemicals are now reported for the first time. Trapping tests carried out in the black currant field revealed that E2,Z13-18:OAc, when tested separately, attracted S. tipuliformis males, while addition of E3,Z13-18:OAc to the main component increased the effectiveness of E2,Z13-18:OAc over seven times. The attractiveness of 6 component lures did not differ significantly from the one of the binary mixture, confirming that E2,Z13-18:OAc and E3,Z13- 18:OAc in the ratio100:0.7 are essential sex pheromone components of S. tipuliformis. Trapping tests carried out at the dwelling place of Synanthedon scoliaeformis (Borkhausen) (Lepidoptera: Sesiidae) revealed that, in addition to intraspecific synergistic effect, E3,Z13-18:OAc increased the specificity of the pheromone signal of S. tipuliformis, acting by intraspecific mode as an attraction antagonist against S. scoliaeformis males. By this way, it ensured the specificity of the sex attraction signal of the currant borer. Consequently, both compounds E2,Z13-18:OAc and E3,Z13-18:OAc have to be present in pheromone formulations used for monitoring and/or control of S. tipuliformis to avoid effecting non-target species. Other compounds identified from the sex pheromone gland of S. tipuliformis did not show any significant interspecific activity for males of S. scoliaeformis, however, they provide a basis to achieve specificity of a pheromone signal of S. tipuliformis and could act as attraction antagonists against other clearwing moth species which, like S. tipuliformis, employ E2,Z13- 18:OAc as their sex pheromone component.


1997 ◽  
Vol 129 (6) ◽  
pp. 1001-1008 ◽  
Author(s):  
P.J. Silk ◽  
L.P.S. Kuenen ◽  
A.R. Alford ◽  
G.C. Lonergan ◽  
G.G. Grant

AbstractUsing gas chromatography and gas chromatography – mass spectrometry analyses of sex pheromone gland volatiles, we identified E- and Z-11-tetradecenals (E:Z-11-14:Aid) in an 85:15 blend of E:Z as the primary sex pheromone components of Croesia semipurpurana (Kearfott). Similar chemical analyses of sex pheromone gland extracts indicated the presence of the congeneric acetates (85:15 E:Z-11-14:Ac) and their saturated analogue (14:Ac); in addition, 85:15 E:Z-11-14:Alds were present at 5% of the acetates. The E:Z-11-14:Alds alone elicited trap capture; admixtures of saturated and unsaturated acetate analogues exhibited no significant synergistic or inhibitory effects. PVC rods with an 85:15 E:Z-11-14:Ald blend is recommended as a trap bait for monitoring population trends. It is unknown whether or not the components identified here represent the complete pheromone blend of this species; data from traps suspended 1.5 m above the ground versus those suspended 10 m above the ground suggest that future field studies may need to be conducted with traps positioned in the tree canopy.


1984 ◽  
Vol 116 (5) ◽  
pp. 777-779 ◽  
Author(s):  
P. E. A. Teal ◽  
J. H. Tumlinson ◽  
J. R. McLaughlin ◽  
R. Heath ◽  
R. A. Rush

Fourteen and 16 carbon saturated and monounsaturated aldehydes have been identified as sex pheromone components for the four. species of Heliothis studied to date (Nesbitt et al. 1979; Klun et al. 1979; Teal et al. 1981). With the exception of H. zea (Boddie), the alcohol corresponding to the major aldehyde component, (Z)-1 l-hexadecen- 1-ol (Zl l-16:OH), also has been found in pheromone gland extracts of all species. We report here the identification of Zll-16:OH from pheromone gland extracts of H. zea females and the results of field trapping studies used to assess the behavioral effects of this compound on conspecific males.


ChemBioChem ◽  
2015 ◽  
Vol 16 (7) ◽  
pp. 1047-1051 ◽  
Author(s):  
Jana Brabcová ◽  
Zuzana Demianová ◽  
Jiří Kindl ◽  
Iva Pichová ◽  
Irena Valterová ◽  
...  

2005 ◽  
Vol 31 (3) ◽  
pp. 621-646 ◽  
Author(s):  
A. M. El-Sayed ◽  
A. R. Gibb ◽  
D. M. Suckling ◽  
B. Bunn ◽  
S. Fielder ◽  
...  

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