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  • 1
    Electronic Resource
    Electronic Resource
    Specificity of communication channels in four limacodid moths: Darna bradleyi, Darna trima, Setothosea asigna, and Setora nitens (Lepidoptera: Limacodidae) (2000)
    Springer
    Chemoecology 10 (2000), S. 193-199 
    Details
    ISSN: 1423-0445
    Keywords: Key words.Darna bradleyi–Darna trima–Setothosea asigna–Setora nitens– nettle caterpillars – oil palm –Elaeis guineensis– antagonism – diel periodicity – habitat partitioning – sex pheromone – communication channel – reproductive isolation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary. Darna bradleyi Holloway, D. trima Moore, Setothosea asigna van Eecke and Setora nitens Walker are sympatric and coseasonal limacodid moths in plantations of oil palm, Elaeis guineensis Jacq. (Arecales: Palmae), in Borneo, southeast Asia. We tested the hypothesis that these four species maintain reproductive isolation through specificity in diel periods of communication, microlocation for communication and/or communication signal (pheromone). Studying diel periodicity of calling behavior by female moths and response by male moths to traps baited with virgin females or synthetic pheromone, we determined that sexual communication of D. bradleyi and D. trima took place from ˜17:30 to 18:45 hr and that of S. asigna and S. nitens from ˜18:45 to 20:00 hr and from ˜18:30 to 19:30 hr, respectively. Over 80% of male S. asigna and S. nitens were captured in pheromone-baited traps suspended 〉5 m high, whereas male D. bradleyi and D. trima were captured mostly in traps 〈5 m high. Synthetic pheromone baits attracted male moths in a species-specific manner. Moreover, baits containing both S. asigna and S. nitens pheromones failed to attract any male moths, indicating that female S. asigna and S. nitens, with overlapping communication periods, use bifunctional pheromone components that attract conspecific males while repelling heterospecifics. Similarly, addition of D. bradleyi pheromone to S. asigna or S. nitens pheromone reduced attraction of male S. asigna and S. nitens. The failure of D. bradleyi and D. trima, which overlap in time and microlocation for communication, to evolve bifunctional pheromones may be attributed to the recent occurrence of sympatry between D. bradleyi and D. trima in Borneo, apparently too recent for bifunctional pheromones to have evolved. We conclude that D. bradleyi, D. trima, S. asigna and S. nitens utilize any or all of diel periodicity, intra and interspecific effects of communication signal and/or microlocation for signaling, allowing these limacodids to co-inhabit the same habitat and remain reproductively isolated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/PL00001822
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  • 2
    Electronic Resource
    Electronic Resource
    Sex Pheromone Components of Nettle Caterpillar, Setora nitens (2000)
    Springer
    Journal of chemical ecology 26 (2000), S. 1983-1990 
    Details
    ISSN: 1573-1561
    Keywords: Setora nitens ; Setothosea asigna ; nettle caterpillar ; Limacodidae ; Lepidoptera ; sex pheromone ; (Z)-9-dodecenal ; (Z)-9,11-dodecadienal ; (E)-9-dodecenal ; (E)-9,11-dodecadienal ; oil palm ; Elaeis guineensis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Gas chromatographic–electroantennographic detection (GC-EAD) analyses of pheromone gland extracts of female nettle caterpillars, Setora nitens, revealed four compounds that consistently elicited responses from male moth antennae. Retention indices on three fused silia columns (DB-5, DB-23, and DB-210) of two EAD-active compounds were almost identical to those of (E)-9-dodecenal (E9–12 : Ald) and (E)-9,11-dodecadienal (E9,11–12 : Ald), two pheromone components previously identified in congeneric Setothosea asigna. However, comparative GC, GC-EAD, and GC-mass spectrometry of extracted S. nitens compounds and authentic standards revealed that the candidate pheromone components were (Z)-9-dodecenal (Z9–12 : Ald) and (Z)-9,11-dodecadienal (Z9,11–12 : Ald). The two other EAD-active compounds in pheromone gland extracts proved to be the corresponding alcohols to these aldehydes. In field-trapping experiments in Tawau, Malaysia, synthetic Z9–12 : Ald and Z9,11–12 : Ald at a 1 : 1 ratio, but not singly, attracted male S. nitens. Attractiveness of these two aldehydes could not be enhanced through the addition of their corresponding alcohols. Whether these differences in pheromone biology and chemistry between S. nitens and S. asigna are sufficient to prevent cross-attraction of heterospecific males or whether nonpheromonal mechanisms are required to maintain reproductive isolation is currently being studied.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1005513211225
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  • 3
    Electronic Resource
    Electronic Resource
    Identification of Sex Pheromone Components of Nettle Caterpillar, Setothosea asigna (1997)
    Springer
    Journal of chemical ecology 23 (1997), S. 2187-2196 
    Details
    ISSN: 1573-1561
    Keywords: Setothosea asigna ; nettle caterpillar ; Limacodidae ; Lepidoptera ; sex pheromone ; (E)-9-dodecenal ; (E)-9,11-dodecadienal ; oil palm ; Elaeis guineensis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Gas chromatographic–electroantennographic detection (GC-EAD) analyses of female nettle caterpillar, Setothosea asigna, pheromone gland extracts revealed seven antennally active compounds. Based on their retention indices on three fused silica columns (DB-5, DB-23, and DB-210), these compounds were hypothesized and, through comparative GC, GC-EAD and GC-mass spectrometry with authentic standards, confirmed to be Δ10-undecenal, dodecanal, (E)-9-dodecenal (E9–12:Ald), (Z)-9-dodecenal, (E)-9-dodecen-1-ol, (E)-9,11-dodecadienal (E9,11–12:Ald), and (E)-9,11-dodecadienol. E9–12:Ald and E9,11–12:Ald were most abundant in female S. asigna pheromone extracts. In field trapping experiments in Palembang, Indonesia, synthetic E9–12: Ald and E9,11–12:Ald at a 1:1 ratio, but not singly, attracted S. asigna males. Attractiveness of these two aldehydes could not be enhanced further through the addition of their corresponding alcohols and/or other aldehydic candidate pheromone components. Use of E9–12:Ald and E9,11–12:Ald for pheromone-based monitoring of S. asigna populations will require lure formulations that minimize pheromone degradation by ultraviolet radiation and atmospheric oxidation.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/B:JOEC.0000006438.03728.1a
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  • 4
    Electronic Resource
    Electronic Resource
    Decadienoates: Sex Pheromone Components of Nettle Caterpillars Darna trima and D. bradleyi (2000)
    Springer
    Journal of chemical ecology 26 (2000), S. 1969-1981 
    Details
    ISSN: 1573-1561
    Keywords: Lepidoptera ; Limacodidae ; Darna trima ; Darna bradleyi ; Setothosea asigna ; Setora nitens ; nettle caterpillars ; oil palm ; sex pheromone ; 2-methylbutyl (E)-7,9-decadienoate ; (E)-2-hexenyl (E)-7,9-decadienoate ; methyl (E)-7,9-decadienoate ; isobutyl (E)-7,9-decadienoate ; (E)-9dodecenal ; (E)-9,11-dodecadienal ; (Z)-9-dodecenal ; (Z)-9,11-dodecadienal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract This study was undertaken to identify sex pheromone components of nettle caterpillars Darna trima and Darna bradleyi (Lepidoptera: Limacodidae) whose larvae defoliate oil palm, Elaeis guineensis, in southeast Asia. Coupled gas chromatographic–electroantennographic detection (GCEAD) analyses of pheromone gland extracts revealed two antennally active compounds produced by female D. trima and two by female D. bradleyi. Molecular structures of these candidate pheromone components were identified by electron-impact and chemical-ionization mass spectrometry; retention-index calculations on DB-5, DB-23, and DB-210 columns; microanalytical treatments, as well as syntheses of "auxilliary" compounds that facilitated identification of the compounds. The compounds from D. trima were 2-methylbutyl (E)-7,9-decadienoate (A) and (E)-2-hexenyl (E)-7,9decadienoate (B); from D. bradleyi we identified methyl (E)-7,9-decadienoate (C), and isobutyl (E)-7,9-decadienoate (D). In field experiments in Malaysia, (S)-2-methylbutyl (E)-7,9-decadienoate (SA) in combination with B proved to be essential and synergistic pheromone components for attraction of male D. trima. (R)-2-Methylbutyl (E)-7,9-decadienoate (RA) had no behavioral activity. Compound D singly attracted male D. bradleyi, but addition of C to D at a 1 : 10 ratio significantly enhanced attractiveness of the bait. Synthetic pheromone blends were more effective trap baits than unmated female moths and could be developed for monitoring populations of D. trima and D. bradleyi in Asian oil palm plantations.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1005561127155
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