A Male Sex Pheromone in a Scorpionfly

It has been postulated that males of a number of scorpionfly species produce sex pheromones. This is based on the observation that females often respond only to conspecific males when they evert their genital pouch, the proposed site of pheromone release. In this study, we prove that in Panorpa germanica (Mecoptera, Panorpidae), the eversion of a male’s genital pouch is associated with the release of a volatile sex pheromone. In dual choice situations, females showed a high preference for ‘calling’ (males with everted genital pouch) over noncalling individuals. Volatiles emitted by males and females were collected and identified by coupled gas chromatography–mass spectrometry. Two aldehydes [(2E,6Z)-nona-2,6-dienal and (E)-non-2-enal] were characteristic of calling males but not of noncalling or immature males or females. Bioassays with synthetic compounds confirmed that the identified substances are attractive to females. To the best of our knowledge, this is the first identification of a sex pheromone in scorpionflies.     

Characterization of a Female-Produced Courtship Pheromone in the Parasitoid Nasonia vitripennis

Males of the parasitoid Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae) show a characteristic courtship behavior. We demonstrate that male arrestment and key behavioral elements of the courtship sequence are mediated by a female-derived contact sex pheromone. Males were arrested on paper disks treated with female extracts but not on those treated with male extracts. Male responsiveness was influenced by the surface to which female extracts were applied. Extracts applied to an extracted beetle elytron arrested males more strongly than those applied to filter paper of comparable size. However, more complex behavioral elements, such as head nodding and copulation attempts, were shown only when extracts were applied to extracted male cadavers, suggesting that tactile or visual cues synergize the male response. The chemicals involved are stable, of low volatility, and nonpolar. Dead females arrested males and elicited courtship behavior for at least 8 d. Males showed no sign of attraction to live females at a distance of 3 cm in an olfactometer. Fractionation of female extracts demonstrated that the activity was exclusively located in the nonpolar fraction. Analysis of the active fraction by gas chromatography–mass spectrometry revealed that cuticular hydrocarbons with chain lengths between 25 and 37 carbon units were present. Comparison of hydrocarbon profiles from males and females showed qualitative and quantitative differences. These results suggest that sex-specific cuticular hydrocarbons are the key signals mediating the male courtship behavior in N. vitripennis.     

Evidence for Four-Component Close-Range Sex Pheromone in the Parasitic Wasp Glyptapanteles flavicoxis

Females of the parasitic wasp Glyptapanteles flavicoxis (Hymenoptera: Braconidae) deposit a close-range sex pheromone from their abdominal tip that attracts conspecific males and elicits wing-fanning behavior. In this study, we isolated the pheromone components and determined their role in the males' behavior. In coupled gas chromatographic–electroantennographic detection (GC-EAD) analyses of the females' body extract, four components (below GC detection) elicited strong responses from male antennae. Monitored by GC-EAD, the components were separated by flash silica gel and high-performance liquid chromatography. Y-tube olfactometer experiments with one or more components revealed that all are necessary to elicit short-range attraction and wing-fanning responses by males. These components remained below detection threshold of the mass spectrometer (∼10 pg) even when 4500 female equivalents were analyzed in a single injection, which attests to the potency of the pheromone and the insects' sensitivity to it.     

Responses of Japanese Giant Looper Male Moth to Synthetic Sex Pheromone and Related Compounds

The Japanese giant looper, Ascotis selenaria cretacea, is a serious defoliator of tea gardens in Japan. In Mie Prefecture male moths were dose-dependently attracted to rubber septa baited with 0.1–10.0 mg of the sex pheromone component (Z,Z)-6,9-cis-3,4-epoxynonadecadiene. Monitoring by pheromone traps showed three flight periods (June, July, and August–September). A septum with a 1-mg dose was still active after exposure for over three months in the field, but the number of males captured by the old lure was one fifth of that captured by a fresh lure. The parent 3,6,9-triene, a minor pheromonal component, showed a synergistic effect on male attraction when mixed with the pheromonal epoxydiene at a very low ratio, but the 1:1 mixture hardly captured any male moths. Attraction was also effectively inhibited by the positional isomers (6,7- and 9,10-epoxydienes), which exhibited rather strong electrophysiological activities on the male antennae. When these related compounds were placed around a trap baited with the synthetic pheromone, the number of captured moths remarkably decreased, which indicates the possibility of using the compounds as a disruptant.     

Potential for Use of Synthetic Sex Pheromone for Mating Disruption of the Olive Pyralid Moth, Euzophera pinguis

The potential for pheromone-based mating disruption of the olive pyralid moth (OPM), Euzophera pinguis, in olive groves was investigated during the second flight period in small-plot trials in 2002. The female of this species emits a blend of (9Z,12E)-tetradecadien-1-ol and (9Z,12E)-tetradecadienyl acetate, which were synthesized for field tests. Mating disruption efficacy in 0.8-ha trials was evaluated using two parameters: reduction of male capture in pheromone traps and reduction of infestation in infestation-prone sites. White rubber septa containing 10 mg of pheromone blend as disruptant were applied at a density of 50 septa/ha for each treatment. Mean catches of E. pinguis males in pheromone traps were greatly reduced (> 95%) in pheromone-treated plots relative to similar traps placed in control plots. In addition, significant reductions were recorded (35-40%) in the oviposition and infestation levels during pheromone treatment. The total amount of pheromone blend released from disruption dispensers during the field trials was estimated to average 5.4 mg/ha/day, over 56 days.     

4-Methylquinazoline is a Minor Component of the Male Sex Pheromone in <Emphasis Type="Italic">Nasonia vitripennis</Emphasis>

We identified 4-methylquinazoline (4-MeQ) as a minor component of the male sex pheromone of the parasitoid Nasonia vitripennis. Like the major components (4R,5R)- and (4R,5S)-5-hydroxy-4-decanolide (HDL), 4-MeQ is synthesized in the abdomen of males. At doses of 6 or 1 ng, 4-MeQ synergized the response of virgin females to the HDL-diastereomers in a still-air olfactometer, but was not attractive as a single component. 4-MeQ is also responsible for the characteristic medicinal odor of N. vitripennis males.     

Reinvestigation of Female Sex Pheromone of Processionary Moth (Thaumetopoea pityocampa): No Evidence for Minor Components

The female sex pheromone of the processionary moth Thaumetopoea pityocampa has been reinvestigated to look for possible minor components. Examination by GC-MS and GC-EAD of the contents of virgin female glands, after stimulation with PBAN (pheromone-biosynthesis-activating neuropeptide), showed that the major component, (Z)-13-hexadecen-11-ynyl acetate (1), appears to be the only pheromone compound present in the gland. Comparison of female attractivity with that of the natural extract and synthetic (Z)-13-hexadecen-11-ynyl acetate showed that this chemical is able to elicit a similar activity to that displayed by virgin females in a wind tunnel. In single cell recording experiments, two specialist receptor cell types were found in the trichoid sensilla. One cell type was tuned to enyne acetate 1. The other one was tuned to (Z,Z)-11,13- hexadecadienal and (Z)-13-hexadecen-11-ynal, the major components of the pheromone blend of other Thaumetopoea spp., and constitutes a further example of interspecific inhibitor receptor cells. Our results show that the processionary moth may not need minor components for successful mate recognition.     

Evidence for a Male-Produced Sex Pheromone in the Western Flower Thrips Frankliniella occidentalis

Olfactometer bioassays of walking adult western flower thrips Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae) showed that virgin females (1- to 3-d postemergence) were attracted to the odor of 25 adult males, but not to the odor of 25 adult females, providing behavioral evidence for a male-produced sex pheromone in this species. In contrast to earlier findings, mixed-age adult males were attracted to the odor of adult males. GC analysis of odors collected on SPME fibers revealed two major components and five minor components that were present in the male odor and not in the female odor. The compounds were not present in hexane extracts of males, indicating that these compounds are produced on demand and not stored.     

Field Trials with the Synthetic Sex Pheromone of the Oak Processionary Moth Thaumetopoea processionea

The biological activity of synthetic (Z,Z)-11,13-hexadecadienyl ace- tate, the major pheromone component found in female gland extracts of the oak processionary moth Thaumetopoea processionea, was evaluated in field trials. Traps baited with 10 mg of the chemical efficiently attracted a large number of males provided they were placed in the upper crown region of the oaks. Devices positioned 10–15 m high in the trees attracted significantly more males than those traps installed at 2 or 6–8 m above the ground. Pherocon traps were slightly more efficient than Delta traps, and lower or higher amounts of the attractant in the baits did not significantly influence the number of moths caught. The importance of the stereomeric purity of the lure and the easy isomerization of the (Z,Z)-acetate to other isomers, particularly to the E,E isomer, should be considered for the development of efficient formulations in the field.     

Behavioral Evidence for a Contact Sex Pheromone Component of the Emerald Ash Borer, <Emphasis Type="Italic">Agrilus Planipennis</Emphasis> Fairmaire

The cuticular hydrocarbon profiles of emerald ash borers, Agrilus planipennis, were examined to determine if there are differences in these compounds between the sexes. We also assessed feral male EAB in the field for behavioral changes based on the application of a female-specific compound to dead, solvent-washed beetles. Males in the field spent significantly more time attempting copulation with dead, pinned female beetles coated with a three-beetle-equivalent dose of 3-methyltricosane than with solvent-washed beetles or those coated in 3-methyltricosane at lower concentrations. Males in the field spent the most time investigating pinned dead, unwashed female beetles. In the laboratory, sexually mature males were presented with one of several mixtures applied in hexane to filter paper disks or to the elytra of dead female beetles first washed in solvent. Male EAB also spent more time investigating dead beetles treated with solution applications that contained 3-methyltricosane than dead beetles and filter paper disks treated with male body wash or a straight-chain hydrocarbon not found on the cuticle of EAB.     

Identification of the Sex Pheromone of Sesamia cretica Lederer

By using solid phase micro-extraction and gas chromatography–mass spectrometry analyses, a sex pheromone blend for the stem borer, Sesamia cretica Lederer (Lepidoptera, Noctuidae), was identified as consisting of (Z)-9-tetradecen-1-ol (80%), (Z)-9-tetradecen-1-yl acetate (10%), and (Z)-11-hexadecen-1-ol (10%). The first two components had previously been discovered as attractants for S. cretica in field tests, but had not been identified in the female’s sex pheromone gland. A field-trapping trial showed that the three-component blend gave the highest catches of male S. cretica. This blend, in a sticky trap, was used to monitor a population of S. cretica in Iran, allowing the seasonal flight activity of this insect to be compared with that of a sympatric population of S. nonagrioides. The role of pheromones in the reproductive isolation of these species is discussed.     

Pheromone Antagonism in the European Corn Borer Moth Ostrinia nubilalis

Mixing the sex pheromones of the Mediterranean corn borer, Sesamia nonagrioides, and the European corn borer, Ostrinia nubilalis, results in significantly lower captures of O. nubilalis when compared to traps loaded with its pheromone alone. Rubber septa loaded with a constant concentration of the pheromone of O. nubilalis and different percentages of the S. nonagrioides pheromone (from 1 to 100%) causes dose-dependent antagonism in the field. Electroantennograms of O. nubilalis males showed high antennal responses to its own pheromone components, followed by smaller responses to the major, [(Z)-11-hexadecenyl acetate (Z11-16:Ac)], and two minor components [dodecyl acetate (12:Ac) and (Z)-11-hexadecenal (Z11-16:Ald)] of the S. nonagrioides pheromone. There was almost no response to the S. nonagrioides minor component (Z)-11-hexadecenol (Z11-16:OH). Field tests that used traps baited with the O. nubilalis pheromone plus individual components of S. nonagrioides showed that Z11-16:Ald causes the antagonism. Adding 1% Z11-16:Ald to the pheromone of O. nubilalis reduced oriented flight and pheromone source contact in the wind tunnel by 26% and 83%, respectively, and trap captures in the field by 90%. The other three pheromone components of S. nonagrioides inhibited pheromone source contact but not oriented flight of O. nubilalis males and did not inhibit capture in the field. Cross-adaptation electroantennogram suggests that Z11-16:Ald stimulates a different odor receptor neuron than the pheromone components of O. nubilalis. We conclude that Z11-16:Ald is a potent antagonist of the behavioral response of O. nubilalis.     

Female-Produced Sex Pheromone of the Predatory Bug Geocoris punctipes

A compound identified from air-entrained volatiles produced by adult female Geocoris punctipes attracted male bugs and stimulated males to investigate nearby moving objects of the appropriate size in their search for females. The compound was identified as (E)-2-octenyl acetate, a relatively common component of the volatile semiochemicals produced by a number of heteropteran species. This compound comprised a significant proportion of the female volatiles, whereas it was detected in only trace amounts in volatiles collected from live males. Other components in the extracts from adults of both sexes included (E)-2-hexenyl acetate, (E)-2-octenal, and several saturated hydrocarbons, but these components were not part of the attractant. These compounds plus (E)-2-hexenal, (E)-4-oxo-2-hexenal, and (E)-2-decenal were found in extracts of homogenized adults, whereas the cast skins from late instar nymphs contained (E)-2-octenal, (E)-4-oxo-2-octenal, (E)-2-octenoic acid, and several saturated hydrocarbons.     

Sex Pheromone of Ascogaster quadridentata, a Parasitoid of Cydia pomonella

Porapak Q volatile extracts of female Ascogaster quadridentata, an egg-larval endoparasitoid of codling moth, Cydia pomonella, bioassayed in Y-tube olfactometers attracted male, but not female, A. quadridentata. Coupled gas chromatographic–electroantennographic detection (GC-EAD) analysis of bioactive extracts revealed three compounds that elicited responses by male A. quadridentata antennae. GC-mass spectra (MS) indicated, and comparative analyses of authentic standards confirmed, that these compounds were (Z,Z)-9,12-octadecadienal, (Z)-9-hexadecenal, and 3,7,11-trimethyl-6E,10-dodecadienal. (Z,Z)-9,12-Octadecadienal alone attracted laboratory-reared male A. quadridentata in Y-tube olfactometer and field-cage bioassays, and attracted feral A. quadridentata in a field experiment. This sex pheromone could be used to help detect populations of A. quadridentata, delineate their distributions, and determine potential sources of parasitoids for capture and release in integrated programs for control of C. pomonella.     

Evidence for the controlled release of a crustacean sex pheromone

Evidence for the controlled release of a crustacean sex pheromone: mature malePortunus sanguinolentus (Herbst) did not give the characteristic display described by Ryan (1966) to water from a container with a carried or artificially restrained premolt female. However, the sex pheromone was still present in the urine of the restrained female, suggesting that she inhibits the emission of the sex pheromone by regulating her urine flow.Based on part of a dissertation presented by the author in partial fulfillment of the requirements for the doctoral degree in zoology at the University of Hawaii.     

Synthesis and Characterization of 2,13- and 3,13-Octadecadienals for the Identification of the Sex Pheromone Secreted by a Clearwing Moth

In addition to 2,13- and 3,13-octadecadien-1-ols and their acetates, aldehyde analogs have been identified from lepidopteran species in the family Sesiidae. To establish a reliable analytical method for determining the positions and configurations of the two double bonds in natural pheromone components, all geometric isomers of the 2,13- and 3,13-octadecadienals were synthesized by Dess-Martin oxidation of the corresponding alcohols with limited isomerization of the double bond at the 2- or 3-position. GC-MS analysis of these aldehydes showed isomerization of (Z)-2-, (Z)-3-, and (E)-3-double bonds to an (E)-2-double bond, even with a cool on-column injection. In contrast, HPLC analysis with an ODS column was accomplished without isomerization. The geometric isomers of each dienal eluted in the order ZZ → EZ → ZE → EE. The conjugated 2,13-dienals were detectable in nanogram amounts with a UV detector at 235 nm. Whereas the detection of 3,13-dienals was difficult because of the lack of a chromophore, a highly sensitive analysis was achieved after derivatization with 2,4-dinitrophenylhydrazine. LC-MS with atmospheric pressure chemical ionization showed a strong [M-1]^- at m/z 443 for the derivatives. Based on these analytical data, a pheromone extract of a sesiid moth, Macroscelesia japona, was examined by HPLC and LC-MS, and it was confirmed that the octadecadienal tentatively identified by a previous GC-MS analysis did indeed have the 2E,13Z configuration. Furthermore, field evaluation of four synthetic geometric isomers of the 2,13-dienal revealed specific attraction to a lure with the (2E,13Z)-isomer as a main component.     

Identification of a Sex Pheromone Component of Pseudococcus cryptus

A sex pheromone component of Pseudococcus cryptus has been isolated and identified. The crude pheromone extract obtained by airborne collection was fractionated by liquid chromatography (LC) on Florisil, and further purified by high performance liquid chromatography and preparative Gas Chromatography (GC). The pheromone component was shown to be an ester, the alcohol part of which was identical to the known alcohol moiety of the pheromone of Planococcus citri. The chemical structure was determined to be 3-isopropenyl-2,2-dimethylcyclobutylmethyl 3-methyl-3-butenoate by MS and ¹H NMR analyses. The absolute configuration of the pheromone was assigned as (1R,3R) by comparison of the retention time of the alcohol derived from the P. cryptus pheromone with those of the alcohol derived from P. citri pheromone, and a synthetic sample of alcohol enriched in the (1R,3R)-enantiomer, using a chiral GC stationary phase. The structure of the pheromone was confirmed by synthesis, and by bioassays in a glasshouse.     

Identification of Sex Pheromone Components of the Box Tree Pyralid,Glyphodes perspectalis

Analysis of ovipositor extracts of the box tree pyralid, Glyphodes perspectalis (Lepidoptera: Crambidae), by coupled gas chromatography-electroantennogram detection and gas chromatography yielded three candidate pheromone compounds. Gas chromatography-mass spectrometry, and reaction with dimethyl disulfide (DMDS), identified these compounds as (Z)-11-hexadecenal (Z11-16:Ald), (E)-11-hexadecenal (E11-16:Ald), and (Z)-11-hexadecenol (Z11-16:OH). The ratio of these three compounds in crude extract was 5:1.25:1, and the total amount was approximately 100 ng/female. In laboratory bioassays, Z11-16:Ald alone was attractive to males. In field bioassays, however, Z11-16:Ald alone was not attractive to males, but a mixture of Z11-16:Ald and E11-16:Ald was. The addition of Z11-16:OH to the two aldehydes, significantly reduced attractiveness to male moths in a field trial. From these results, we conclude that the aldehyde compounds comprise the sex pheromone components of G. perspectalis. A rubber septum containing 0.6 mg of the two aldehydes at the natural ratio was an effective lure for monitoring this pest.     

(2,3,4,4-Tetramethylcyclopentyl)Methyl Acetate,a Sex Pheromone from the Obscure Mealybug: First Example of a New Structural Class of Monoterpenes

The sex pheromone of the obscure mealybug, Pseudococcus viburni, consists of (1R*,2R*,3S*)-(2,3,4,4-tetramethylcyclopentyl)methyl acetate, the first example of a new monoterpenoid structural motif in which the two isoprene units forming the carbon skeleton are joined by 2'-2 and 3'-4 connections rather than the usual 1'-4, head-to-tail connections. This highly irregular terpenoid structure, and the irregular terpenoid structures of related mealybug species, suggest that these insects may have unique terpenoid biosynthetic pathways.     

Laboratory and Field Study of the Attraction of Male Pea Midges, Contarinia pisi, to Synthetic Sex Pheromone Components

Behavioral activity of the recently identified sex pheromone components of the pea midge, Contarinia pisi, (2S,11S)-diacetoxytridecane, (2S,12S)-diacetoxytridecane, and 2-acetoxytridecane, was tested in wind tunnel and field-trapping experiments. In the wind tunnel, the attractancy of the three-component blend in a 7 : 10 : 0.1 ratio (following the above order, mimicking the ratios found in gland extract) did not differ significantly from female gland extract, whereas a mixture of the two major components (7 : 10) only attracted 2% of the males to the source. In the field, traps baited with the three-component blend caught by far the largest number of males. Traps baited with the two major components only caught slightly more than the blank traps, and catches in traps baited with 2-acetoxytridecane alone did not differ from catches in the blank traps. Traps baited with the racemate of all three components did not catch more than the blank traps, indicating that some of the enantiomers are inhibitory.