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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Entomologia experimentalis et applicata 71 (1994), S. 185-192 
    ISSN: 1570-7458
    Keywords: Lepidoptera ; Pyralidae ; Indianmeal moth ; semiochemicals ; attraction ; oviposition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Substrates contaminated by wandering fifth instar larvae ofPlodia interpunctella (Hübner) (Lepidoptera: Pyralidae) elicit oviposition by conspecific female moths, and larval rearing diet enhances oviposition and also induces upwind flight. Two-choice oviposition assays determined that four-day-old gravid femaleP. interpunctella preferred to lay eggs on dishes containing cornmeal-based rearing diet compared to empty dishes. Pieces of cheesecloth contaminated by fifth instar larvae elicited more oviposition than untreated cheesecloth or dishes with food. The combination of larval contamination and food was preferred over food only or larval contamination only in both two- and four-choice experiments. The factor(s) in larval contamination responsible for eliciting oviposition in female moths was extracted in hexane, confirming that organic semiochemicals are responsible for the effect. The oviposition-eliciting activity of larval contamination was retained on cheesecloth for up to 30 days following treatment with larvae, suggesting the active component(s) is stable and of low relative volatility. In two-choice windtunnel bioassays female moths initiated flight only when rearing food was present in one of the treatments, and they displayed the highest landing responses to a combination of larval contamination and food. Earlier work onP. interpunctella and related pyralid species found that larval contamination due to secretions from the mandibular glands acted as both a spacing pheromone for wandering larvae and as a kairomone for host-seeking parasitoid wasps. The present study suggests that the same or a similar secretion acts as an oviposition-eliciting pheromone for conspecific females.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 16 (1990), S. 2771-2786 
    ISSN: 1573-1561
    Keywords: Colias ; Lepidoptera ; Pieridae ; courtship pheromone ; pheromone variation ; pheromone production ; cuticular hydrocarbons ; n-heptacosane ; 13-methylheptacosane ; n-nonacosane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Body size, age, ambient temperature, wing wear, and flight activity were investigated as possible sources of variation in the quantities and relative proportions of the three chemical components [n-heptacosane (C27), 13-methylheptacosane (13MH), andn-nonacosane (C29)] of the male courtship pheromone ofColias eurytheme butterflies. Size of the male has very little influence on the amount of any of the pheromone components present on the wings. Most of the deposition of all three components onto the surface of the hindwing occurs between 3 and 9 hr after emergence from the pupa. 13MH is deposited more rapidly than C27 and C29, and C27 more rapidly than C29. After the first 12 hr posteclosion, the pheromone phenotype of an individual male remains relatively constant through at least 96 hr of age. Experiments showed that none of the three chemicals volatilize to any appreciable extent at temperatures likely to be experienced in the field. The pheromones of actively searching and courting males did not differ from those of less-active feeding and resting males, suggesting that volatilization induced by flight activity is not an important source of pheromone variation. Loss of scales with age does seem to affect pheromone phenotype, but not in a readily interpretable way. Although the quantity of 13MH was lower in worn males than in fresh, C27 was higher.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 16 (1990), S. 2755-2770 
    ISSN: 1573-1561
    Keywords: Colias ; Lepidoptera ; Pieridae ; courtship pheromone ; pheromone variation ; cuticular hydrocarbons ; n-heptacosane ; 13-methylheptacosane ; n-nonacosane ; heritability ; genetic correlation ; gas chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The courtship pheromone ofColias eurytheme butterflies varies greatly among males in both the quantities and relative proportions of its three chemical components [n-heptacosane (C27), 13-methylheptacosane (13MH),n-nonacosane (C29)]. Narrow-sense heritabilities were high for the blend of 13MH and C27 and for the component quantities in one population (Kansas) but were low for the other population tested (Arizona). Genetic correlations between the three components were high in both populations, indicating a substantial degree of additive genetic influence on the component blends. High variability among populations in phenotypic correlations suggests that much of the male-to-male variation in the courtship pheromone may be attributable to environmental or developmental sources. Pheromone phenotypes do not seem to be associated with alba genotype.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 12 (1986), S. 385-409 
    ISSN: 1573-1561
    Keywords: Lepidoptera ; pheromone ; chirality ; epoxide ; hydroxydanaidal ; biosynthesis ; polyene ; alkaloid ; Creatonotos transiens ; Creatonotos gangis ; Arctiidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The two major components of the female sex pheromones of twoCreatonotos species have been identified as an achiral C21 triene, (Z,Z,Z)-3,6,9-heneicosatriene, and a chiral epoxide, (Z,Z)-2(2,5-octadienyl)-3-undecyloxirane. The ratios of these components in the two species fall into nonoverlapping ranges. Two additional achiral minor components, (Z,Z)-6,9-heneicosadiene and (Z,Z,Z)-3,6,9-tricosatriene, were also identified in the female sex gland extracts. The male pheromone of both species consists of hydroxydanaidal, a chiral dihydropyrrolizine derived from pyrrolizidine alkaloids in the larval diet.Creatonotos transiens was found to convert dietary heliotrine into (R)-(−)-hydroxydanaidal, with inversion at the single asymmetric carbon atom. The possible biological and biosynthetic significance of the chiral pheromone components are discussed, and they are compared with known examples of chiral lepidopteran pheromones.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-1561
    Keywords: Currant borer ; Synanthedon tipuliformis ; Lepidoptera ; Sesiidae ; (E,Z)-2,13-octadecadien-1-ol acetate ; (E,Z)-3,13-octadecadien-1-ol acetate ; (Z,Z)-3,13-octadecadien-1-ol acetate ; sex pheromone ; trapping synergist ; trapping inhibitor ; field trapping ; sexual behavior ; geographically isolated populations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Various blends of (E,Z)-2,13-octadecadien-1-ol acetate (E,Z2,13-18: OAc), (Z)-13-octadecen-1-ol acetate (ZOAc) (two previously identified pheromone components of the currant borer,Synanthedon tipuliformis females), (E,Z)-, (Z,Z)-3,13-octadecadien-1-ol acetates (E,Z- andZ,Z3,13–18:OAc), andZ,Z-3,13-octadecadien-1-ol (Z,Z3,13–18:OH) were evaluated in field traps in three geographic regions. MaleS. tipuliformis were attracted toE,Z2,13–18:OAc in Tasmania, New Zealand, and Hungary. Captures were not influenced by the addition ofZ13–18: OAc, tested in Tasmania and Hungary. In Hungary and New Zealand, the addition ofE,Z3,13–18: OAc toE,Z2,13–18:OAc in a ratio of 100:3 was strongly synergistic; however, in Tasmania captures were reduced. The addition ofZ,Z3,13–18: OAc toE,Z2,13–18:OAc in a ratio of 10∶1 resulted in strong inhibition of trap captures in Hungary. WhenZ,Z3,13–18: OAc was added in different ratios to a 100:3 binary mixture ofE,Z2,13–18:OAc/E,Z3,13–18:OAc in Hungary, it strongly reduced captures at, or above a ratio of 100∶3∶3 but no decrease was recorded at a ratio of 100∶3∶1. In New Zealand and Tasmania it reduced captures at a ratio of 100∶3∶1. Observations of behavioral responses of maleS. tipuliformis in Hungary to synthetic baits in the field showed thatE,Z2,13–18:OAcby itself evoked close-range approaches to the source from only 20% of males, whereas the addition ofE,Z3,13–18:OAc in a ratio of 100∶3 raised that value to 65 %. Landing on the source was significant only at sources with a 100∶3∶0.1∶3∶10 blend ofE,Z2,13–18:OAc/E,Z3,13–18: OAc/Z,Z3,13–18: OAc/Z,Z3,13–18: OH/Z13–18: OAc. A 100∶3 binary mixture ofE,Z2,13–18:OAc/E,Z3,13–18:OAc in a dose range of 10–1000 μg can be recommended for more effective field monitoring ofS. tipuliformis populations in Hungary and in New Zealand. In Tasmania, at present,E,Z2,13–18: OAc by itself is the most potent sex attractant of the species.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 26 (2000), S. 2549-2555 
    ISSN: 1573-1561
    Keywords: Lepidoptera ; Carposinidae ; (Z)-12–nonadecen-9–one ; chemical identification ; trapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The female-produced sex pheromone of the New Zealand raspberry budmoth, Heterocrossa rubophaga, was investigated. Gas chromatographic–mass spectrometric analyses revealed the ketone, (Z)-12–nonadecen9–one (Z12–19–9–one). This compound had previously been found in extracts of the sex pheromone gland of the only other carposine moth for which a sex pheromone has been identified, Carposina niponensis, although its effect on the behavior of C. niponensis males had not been established. Field trapping trials in berry fruit gardens showed this compound to elicit high catches of male H. rubophaga, with the catch appearing to plateau (and perhaps decrease) above a dosage of 300 μg on a red rubber septum. In an analysis of an extract of female H. rubophaga sex pheromone glands, there was a suggestion that the homologous (Z)-7–eicosen-11–one, the known sex pheromone component of C. niponensis, was also present. However this could not be established unequivocally and, in a field trial, addition of a small amount of this compound to Z12–19–9–one resulted in no significant increase in trap catch relative to traps baited with Z12–19–9–one alone.
    Type of Medium: Electronic Resource
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