Role of (3<Emphasis Type="Italic">Z</Emphasis>,6<Emphasis Type="Italic">Z</Emphasis>,8<Emphasis Type="Italic">E</Emphasis>)-Dodecatrien-1-ol in Trail Following,Feeding, and Mating Behavior of <Emphasis Type="Italic">Reticulitermes hesperus</Emphasis>

Trail pheromones mediate communication among western subterranean termites, Reticulitermes hesperus Banks. Repetitive passages of ≥28 termites were required to establish a pheromone trail and trails needed to be reinforced because they lasted <48 hr. The minimal threshold concentration for inducing responses from termite workers and secondary reproductives was between 0.01 and 0.1 fg/cm of (3Z,6Z,8E)-dodecatrien-1-ol (henceforth, dodecatrienol). Workers showed optimal trail-following behavior to dodecatrienol at a concentration of 10 fg/cm. Trails with concentrations >10 pg/cm were repellent to workers. Workers did not detect pheromone gradients, responding equally to increasing or decreasing gradients of dodecatrienol, and termite workers were not able to differentiate between different concentrations of dodecatrienol. Termites preferred dodecatrienol trails to 2-phenoxyethanol trails. Antennae played a key role in trail pheromone perception. Dodecatrienol acted as an arrestant for worker termites (10 fg/cm²) and male alates (5 ng/cm²), whereas sternal gland extracts from females attracted male alates. Workers and alates, upon contact with filter paper disks treated with higher doses (10 fg/cm² and 5 ng/cm², respectively) of dodecatrienol, were highly excited (increased antennation and palpation) and repeatedly returned to the treated disks. Dodecatrienol did not act as a phagostimulant when offered on a paper towel disk. Reticulitermes hesperus is highly responsive to dodecatrienol, and it may play an important role in orientation of workers and alates.     

Trail-Following Pheromones in Basal Termites, with Special Reference to Mastotermes darwiniensis

In the framework of an evolutionary study, trail pheromones have been studied in the most basal extant termite, Mastotermes darwiniensis (Mastotermitidae), and two other basal termites, the Termopsidae Porotermes adamsoni (Porotermitinae) and Stolotermes victoriensis (Stolotermitinae). Although workers of M. darwiniensis do not walk in single file while exploring a new environment under experimental conditions and are unable to follow artificial trails in ‘open field’ experiments, they do secrete a trail-following pheromone from their sternal glands. This unique behavior might reflect a primitive function of communication of the sternal gland. The major component of the pheromone appears to be the same in the three basal species: the norsesquiterpene alcohol (E)-2,6,10-trimethyl-5,9-undecadien-1-ol. This represents a new chemical category of trail-following pheromones for termites. The quantity of pheromone was estimated as 20 pg/individual in M. darwiniensis, 700 pg/individual in P. adamsoni, and 4 pg/individual in S. victoriensis. The activity threshold was 1 ng/cm in M. darwiniensis and 10 pg/cm in P. adamsoni. In M. darwiniensis, the trail pheromone was secreted by sternal gland 4 and to a lesser degree by sternal gland 3, sternal gland 5 being almost inactive. This study highlighted phylogenetic relationships between the Mastotermitidae and two subfamilies of the Termopsidae, the Porotermitinae and the Stolotermitinae. Furthermore, it indicated a heterogeneity within the Termopsidae, with Porotermitinae and Stolotermitinae on one hand, and Termopsinae on the other. Finally, Mastotermitidae and Termopsidae, with C14 trail pheromones, are clearly separated from the Kalotermitidae, Rhinotermitidae, and Termitidae that secrete C12 or C20 trail pheromones.     

(Z,Z,E)-3,6,8-Dodecatrien-1-ol, A Major Component of Trail-Following Pheromone in Two Sympatric Termite Species Reticulitermes lucifugus grassei and R. santonensis

Trail-following bioassays show that trails of the two subterranean termites, Reticulitermes lucifugus grassei and R. santonensis, which are sympatric in some areas of southwestern France, are not species specific. Even when tested just above threshold level, trails from pentane extracts of whole workers of R. santonensis are always preferred by both species. If the R. santonensis extract is progressively diluted, the preference is lost. In purified extracts of workers of R. lucifugus grassei that elicited a trail-following response, only one compound is active. It was identified by GC-MS as the same major compound of the trail-following pheromone of R. santonensis: (Z,Z,E)-3,6,8-dodecatrien-1-ol (DTE-OH). The threshold concentration of activity of synthetic DTE-OH was determined to be 10^–3 ng/cm of trail; optimal activity was obtained at 10^–2 ng/cm of trail. The increase of trail-following activity of worker extracts of R. lucifugus grassei after hydrolysis by potassium hydroxide suggests that DTE-OH also is bound to other components in sternal gland secretions. DTE-OH was also identified in alates of R. lucifugus grassei, suggesting that the compound functions both as a trail-following and a sex pheromone, as has been shown to be the case in R. santonensis. This demonstrates the high economy developed by termites in their strategies of chemical communication.     

Major Sex Pheromone Component of Female Herald Moth Scoliopteryx libatrix is the Novel Branched Alkene (6Z,13)-Methylheneicosene

The major component of the female-produced sex pheromone of Scoliopteryx libatrix has been characterized by chemical analysis, synthesis, electrophysiological studies and field tests as (6Z,13)-methylheneicosene, probably the 13S-isomer. This is the first example of a branched chain alkene as a sex pheromone in the Noctuidae and is markedly different from the pheromones of other members of the family. The systematic position of S. libatrix, belonging to a monotypic genus of a one-member subfamily within the Noctuidae, may reflect the unusual structure of the sex pheromone.     

Sex Pheromone Components of Indian Gypsy Moth, <Emphasis Type="Italic">Lymantria obfuscata</Emphasis>

The Indian gypsy moth, Lymantria obfuscata (Lepidoptera: Lymantriidae), has been recognized as a distinct species since 1865 but closely resembles a diminutive form of gypsy moth, Lymantria dispar. We tested the hypothesis that the sex pheromones of L. obfuscata and L. dispar are similar. In laboratory mate acceptance studies, very few male L. dispar made copulatory attempts when paired with female L. obfuscata, suggesting that female L. obfuscata emit one or more pheromone components antagonistic to male L. dispar. In coupled gas chromatographic–electroantennographic detection (GC–EAD) analyses of pheromone gland extract of female L. obfuscata, (Z)-2-methyloctadec-7-ene (2Me-7Z-18Hy) and (7R,8S)-cis-7,8-epoxy-2-methyloctadecane [(+)-disparlure] were most abundant and elicited the strongest responses from male L. obfuscata antennae. In field experiments near Solan (Himachal Pradesh, India), 2Me-7Z-18Hy and (+)-disparlure in combination attracted more male L. obfuscata than did either component alone. This two-component sex pheromone contrasts with the single-component sex pheromone [(+)-disparlure] of L. dispar. The contrasting composition of the lymantriid communities inhabited by L. obfuscata and L. dispar may explain why 2Me-7Z-18Hy is a pheromone component in L. obfuscata and a pheromone antagonist in L. dispar and why (−)-disparlure reduces pheromonal attraction of male L. dispar but not male L. obfuscata.     

Sex Pheromone of <Emphasis Type="BoldItalic">Agriotes acuminatus</Emphasis> (Stephens, 1830) (Coleoptera: Elateridae)

The click beetle species Agriotes acuminatus is distributed in open deciduous forests throughout a large area in Europe. In order to identify its sex pheromone, gland extracts of female beetles were investigated by using GC/MS. Neryl butanoate and 2,6-dimethyl-(Z,E)-2,6-octadien-1,8-diol dihexanoate, in a ratio of approximately 1:5, were the only volatile compounds present in the extracts. Structures of both esters were confirmed by synthesis. Field experiments revealed a strong attraction of A. acuminatus males towards neryl butanoate, which could be synergistically enhanced by addition of 2,6-dimethyl-(Z,E)-2,6-octadien-1,8-diol dihexanoate. The latter compound alone did not show any attractive effect. While all Agriotes spp. investigated to date use geranyl and/or (E,E)-farnesyl esters as sex pheromones, the nerol derivatives of A. acuminatus are the first (Z)-2-configurated pheromones within this genus.     

Semiochemical Investigations of the Insidious Flower Bug, <Emphasis Type="Italic">Orius insidiosus</Emphasis> (Say)

Females of the insidious flower bug, Orius insidiosus (Say) (Hemiptera: Heteroptera: Anthocoridae), produce a volatile sex pheromone and a non-volatile trail pheromone. The sex pheromone consists of the female-specific compound, (E)-2,7-octadienal, and a compound emitted by both sexes, (E)-2-octenal. A synthetic blend of octadienal and octenal weakly, but significantly, attracted O. insidiosus males to sticky traps in the field. The trail pheromone is somehow deposited by O. insidiosus females on the substrate as they walk, and, once contacted, stimulates conspecific adults to search in the vicinity. O. insidiosus males most likely respond to the trail pheromone as the ultimate means to locate potential mates, whereas the benefit of females responding to the trail pheromone may be that this signal acts as a cue indicating the likelihood of finding nearby prey. The O. insidiosus trail pheromone compounds were not identified. The volatile and non-volatile pheromones of O. insidiosus, along with prior research demonstrating that Orius and other anthocorids frequently exploit prey-associated odors as kairomones that guide their foraging, highlight the extent to which the minute pirate bugs use chemical communication. The semiochemistry of the Anthocoridae, particularly their reliance on non-volatile pheromones and kairomones, reinforces the emerging realization that other terrestrial heteropterans also substantially communicate via contact chemoreception, although this communicative channel has not been thoroughly investigated. Mention of commercial products does not constitute an endorsement by USDA.     

Identification of the Sex Pheromone of a Protected Species,the Spanish Moon Moth <Emphasis Type="BoldItalic">Graellsia isabellae</Emphasis>

Sex attractant pheromones are highly sensitive and selective tools for detecting and monitoring populations of insects, yet there has been only one reported case of pheromones being used to monitor protected species. Here, we report the identification and synthesis of the sex pheromone of a protected European moth species, Graellsia isabellae (Lepidoptera: Saturniidae), as the single component, (4E,6E,11Z)-hexadecatrienal. In preliminary field trials, lures loaded with this compound attracted male moths from populations of this species at a number of widely separated field sites in France, Switzerland, and Spain, clearly demonstrating the utility of pheromones in sampling potentially endangered insect species.     

Response of Mythimna unipuncta Males to Components of the Sesamia nonagrioides Pheromone

Several sympatric lepidopteran species feed on maize plants, and the different components of their species-specific female sex pheromones may play a role in attracting conspecifics and/or deter heterospecific males. In this study, we analyzed the content of Mythimna unipuncta pheromone glands and tested the response of males to components of their own pheromone blend and that of Sesamia nonagrioides in the wind tunnel. Whole pheromone glands, and lures where (Z)-9-hexadecenyl acetate, Z)-11-hexadecen-1-ol or (Z)-9-hexadecenyl acetate + (Z)-11-hexadecen-1-ol were added to the major component, (Z)-11-hexadecenyl acetate, elicited significantly higher responses by M. unipuncta males than lures with main component alone, although the levels varied with concentration. In the field a rather different outcome was observed, as the addition of other compounds found in the female pheromone gland did not improve trap catch over lures with only (Z)-11-hexadecenyl acetate. The addition of (Z)-11-hexadecenal, a compound of the S. nonagrioides pheromone, to (Z)-11-hexadecenyl acetate significantly reduced attraction of M. unipuncta males both in the wind tunnel and in the field, as well as the number of sympatric clover cutworm, Discestra trifolii, under field conditions. The addition of (Z)-9-hexadecenyl acetate, a minor component of the M. unipuncta pheromone blend, reduced the number of S. nonagrioides captured in field traps that were baited with the S. nonagrioides lure. The significance of such inhibition in the reproductive isolation of sympatric species that attack maize is discussed.     

A Two-Component Female-Produced Pheromone of the Spider Pholcus beijingensis

Chemical signaling plays an important role in spider sexual communication, yet the chemistry of spider sex pheromones remains poorly understood. Unlike insects and mammals, the identification of spider pheromones has seldom been attempted, and no multicomponent pheromones have been found. Empty webs of sexually receptive females of Pholcus beijingensis were more attractive to male conspecifics as compared to webs of sexually unreceptive females or to mature males. Coincidently, chemical analysis revealed that (E,E)-farnesyl acetate, diisobutyl phthalate, and hexadecyl acetate of the spider webs exhibited higher relative abundances in sexually receptive females than in sexually unreceptive females or males, indicative of possible pheromone components. Two-choice behavioral assays verified that the blend of (E,E)-farnesyl acetate and hexadecyl acetate (w/w: 2:1) attracted males at a dosage equivalent to the amounts of these compounds in one spider web, whereas neither compound alone aroused males. In addition, diisobutyl phthalate (a likely contaminant from contact with plastic) alone or in combination with either of the acetates did not evoke the males’ attraction. The behavioral data suggest that (E,E)-farnesyl acetate and hexadecyl acetate comprise a two-component female-produced sex pheromone in P. beijingensis, the first multicomponent pheromone found in spiders.     

Intra- and Interspecific Activities of Semiochemicals from the Sex Pheromone Gland of the Welsh Clearwing, Synanthedon Scoliaeformis

Analysis of the sex pheromone gland of virgin Synanthedon scoliaeformis females by gas chromatography/mass spectrometry revealed six compounds structurally related to sex pheromone components of other clearwing moths: (E,Z)-2,13-octadecadienyl acetate (E2,Z13-18:OAc), (E,Z)-2,13-octadecadienol, octadecanol acetate, octadecanol, (Z,Z)-3,13-octadecadienyl acetate (Z3,Z13-18:OAc), and (Z)-13-octadecenyl acetate. Trapping tests demonstrated that E2,Z13-18:OAc is the sex pheromone of S. scoliaeformis and is essential for attracting males; addition of the other compounds did not enhance catch. Synanthedon scoliaeformis and S. tipuliformis are the only Palearctic clearwing moths whose distribution range and seasonal flight periods overlap and that are known to use E2,Z13-18:OAc in sex pheromonal communication. Hourly monitoring of male catches in traps revealed that sex pheromone communication in S. scoliaeformis and S. tipuliformis species follows different diurnal patterns. Z3,Z13-18:OAc, found in S. scoliaeformis females, is a known behavioral antagonist against S. tipuliformis males, while (E,Z)-3,13-octadecadienyl acetate, a minor sex pheromone component of S. tipuliformis, is an antagonist against S. scoliaeformis males. The effect of sex pheromones and antagonists, combined with different diurnal mate searching times, contribute to the specificity of sex communication channels in these two clearwing moth species.     

Sex Pheromone of the Saturniid Moth, <Emphasis Type="Italic">Hemileuca burnsi</Emphasis>, from the Western Mojave Desert of California

The sex pheromone blend of Hemileuca burnsi (Lepidoptera: Saturniidae) from the western Mojave Desert was determined to be a combination of (10E,12Z)-hexadecadien-1-yl acetate (E10,Z12-16:Ac), (10E,12Z)-hexadecadien-1-ol (E10,Z12-16:OH), (10E,12E)-hexadecadien-1-yl acetate (E10,E12-16:Ac), and hexadecyl acetate (16:Ac). (10E,12Z)-Hexadecadienal (E10,Z12-16:Ald) was tentatively identified in pheromone gland extracts based on electroantennographic responses and, when added to the above blend, it enhanced trap captures at low doses. The mean ratio of the compounds in extracts of pheromone glands was 100:23:232:14:0.4 (E10,Z12-16:Ac: E10,E12-16:Ac: 16:Ac: E10,Z12-16:OH: E10,Z12-16:Ald). Field trials indicated that although E10,Z12-16:Ac and E10,Z12-16:OH were essential for attraction, the two-component blend was not attractive by itself. Addition of the three other compounds was necessary for maximum attraction, rendering this the most complicated pheromone blend described for a Hemileuca species to date. Similarities between the sex pheromone of H. burnsi and that of the allopatric Hemileuca electra electra and differences between the blends of H. burnsi and that of the sympatric H. electra mojavensis support a case for reproductive character displacement in the pheromone communication channel of H. electra.     

Sex Pheromone of the Dogwood Borer, <Emphasis Type="Italic">Synanthedon scitula</Emphasis>

The sex pheromone of female dogwood borers (DWB) Synanthedon scitula (Harris) (Lepidoptera: Sesiidae) was determined to be an 88:6:6 ternary blend of (Z,Z)-3,13-octadecadienyl acetate (Z,Z-3,13-ODDA), (E,Z)-2,13-octadecadienyl acetate (E,Z-2,13-ODDA), and (Z,E)-3,13-octadecadienyl acetate (Z,E-3,13-ODDA) by gas chromatography–electroantennographic detection (GC–EAD) and gas chromatography–mass spectrometry (GC–MS). The major sex pheromone component, Z,Z-3,13-ODDA, was attractive as a single component. A blend of Z,Z-3,13-ODDA with 1–3% of E,Z-2,13-ODDA (binary blend) was more attractive than the single component. A third component, Z,E-3,13-ODDA, was sometimes observed in GC–EAD analyses, and enhanced attraction to the binary blend in some field bioassays. Lures containing 1 mg of binary and ternary blends attracted 18 and 28 times more male DWB moths, respectively, than caged virgin females in field trials. Attraction was strongly antagonized by addition of as little as 0.5% of E,Z-3,13-octadecadienyl acetate (E,Z-3,13-ODDA). In a period of 12 wk in 2004, more than 60,000 males were captured in sticky traps baited with synthetic pheromone blends in six apple orchards in Virginia, West Virginia, and North Carolina. Lure longevity trials showed that ∼76% of the pheromone remained in rubber septum lures after 12 wk in the field.     

Simultaneous Disruption of Pheromone Communication in Choristoneura rosaceana and Pandemis limitata with Pheromone and Antagonist Blends

In British Columbia, trapping and wind-tunnel studies demonstrated that (Z)-9-tetradecenyl acetate (Z9–14:OAc), a minor component of the sex pheromone for Pandemis limitata, acted as a pheromone antagonist to a sympatric species, Choristoneura rosaceana. Addition of >1% Z9–14:OAc to the four-component C. rosaceana pheromone in a wind tunnel resulted in significant reductions in the proportion of male C. rosaceana that wing fanned, locked on to the plume in flight, oriented upwind, and made source contact, compared to the responses to the pheromone alone. Disruption of pheromone communication was tested in 33.3 × 33.3-m plots, at a release rate of 10 mg/ha/hr using Conrel fiber dispensers. Z9–14:OAc applied alone did not disrupt orientation to virgin-female-baited traps for either C. rosaceana or P. limitata. A 1:1 mixture of Z9–14:OAc and the four-component C. rosaceana pheromone was as effective as the pheromone alone at disrupting orientation of C. rosaceana males to virgin-female-baited traps, demonstrating that disruption apparently did not occur through false-trail following. The 1:1 mixture of Z9–14:OAc and the C. rosaceana pheromone also reduced catches of P. limitata males in virgin-female-baited traps, but not significantly more than the 83% disruption caused by the pheromone alone. Therefore, the C. rosaceana pheromone could be used alone or with Z9–14:OAc to disrupt communication and, presumably, mating in both leafrollers simultaneously.     

A Tetraene Aldehyde as the Major Sex Pheromone Component of the Promethea Moth (Callosamia promethea (Drury))

The promethea moth Callosamia promethea is one of three species of silkmoths from the genus Callosamia that occur in North America. Cross attraction of males to heterospecific calling females has been observed in the field, and hybrid progeny have been produced by pairing heterospecifics in captivity. These observations suggest that all three species share or have considerable overlap in the sex attractant pheromones produced by females, so that other prezygotic isolating mechanisms, such as diel differences in reproductive activity, limit hybridization in the field. Coupled gas chromatography-electroantennogram detection and gas chromatography- mass-spectrometry analyses of extracts of volatiles collected from female promethea moths supported the identification of (4E,6E,11Z,13Z)-hexadeca-4,6,11,13-tetraenal [(4E,6E,11Z,13Z)-16:Ald] as the compound in extracts that elicited the largest responses from antennae of males. The identification was confirmed by non-selective synthesis of several isomers as analytical standards, and stereoselective synthesis of (4E,6E,11Z,13Z)-16:Ald for testing in field trials. Male moths were strongly attracted to synthetic (4E,6E,11Z,13Z)-16:Ald, suggesting that this compound is the major and possibly the only component of the sex pheromone of these large saturniid moths. Based on the cross-attraction of heterospecifics, it is likely that this is also a major pheromone component of the other two North American Callosamia species as well.     

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.     

Reinvestigation of the Sex Pheromone of the Wild Silkmoth Bombyx mandarina: The Effects of Bombykal and Bombykyl Acetate

Sex pheromone investigations of the domesticated silkmoth, Bombyx mori (Lepidoptera: Bombycidae), helped elucidate the molecular and physiological fundamentals of chemical communication in moths, yet little is known about pheromone evolution in bombycid species. Therefore, we reexamined the sex pheromone communication in the wild silkmoth, Bombyx mandarina, which is considered ancestral to B. mori. Our investigations revealed that (a) B. mandarina females produce (E,Z)-10,12-hexadecadienol (bombykol), but not (E,Z)-10,12-hexadecadienal (bombykal) or (E,Z)-10,12-hexadecadienyl acetate (bombykyl acetate), which are pheromone components in other bombycid moths; (b) antennae of male B. mandarina respond strongly to bombykol as well as to bombykal and bombykyl acetate; and (c) bombykal and bombykyl acetate strongly inhibit attraction of B. mandarina males to bombykol in the field. The present study clarifies the evolution of pheromone communication in bombycid moths.     

Support for (Z)-11-Hexadecanal as a Pheromone Antagonist in Ostrinia nubilalis: Flight Tunnel and Single Sensillum Studies with a New York Population

The flight-tunnel response of male Z-strain European corn borer moths (ECB), Ostrinia nubilalis, from a population in New York State (USA), was significantly antagonized by addition of 1% (Z)-11-hexadecanal (Z11-16:Ald) to their sex pheromone (a 97:3 mix of (Z)- and (E)-11-tetradecenyl acetate [Z/E11-14:OAc]). The level of antagonism was equivalent to that observed for the previously identified ECB antagonist, (Z)-9-tetradecenyl acetate (Z9-14:OAc), and supports a recent report showing that Z11-16:Ald, a minor pheromone component of the Noctuid moth, Sesamia nonagrioides, caused antagonism of ECB pheromone communication in sympatric populations in the Iberian Peninsula. Single-sensillum recordings from ECB antennae, which included cross-adaptation experiments, showed that the same olfactory receptor neuron processing Z9-14:OAc inputs was responsible for detecting Z11-16:Ald, and that this neuron was not responsive to two other aldehydes, (Z)-9-tetradecanal (Z9-14:Ald) and (Z)-9-hexadecanal (Z9-16:Ald), found in other moth sex pheromones. Our results show that the antagonism is not confined to one geographic region, is specific for Z11-16:Ald, and that antagonist pathways might have the potential for processing a number of structurally similar compounds.     

New Pheromone Components of the Grapevine Moth <Emphasis Type="Italic">Lobesia botrana</Emphasis>

Analysis of extracts of sex pheromone glands of grapevine moth females Lobesia botrana showed three previously unidentified compounds, (E)-7-dodecenyl acetate and the (E,E)- and (Z,E)-isomers of 7,9,11-dodecatrienyl acetate. This is the first account of a triply unsaturated pheromone component in a tortricid moth. The monoenic acetate (E)-7-dodecenyl acetate and the trienic acetate (7Z,9E,11)-dodecatrienyl acetate significantly enhanced responses of males to the main pheromone compound, (7E,9Z)-7,9-dodecadienyl acetate, in the wind tunnel. The identification of sex pheromone synergists in L. botrana may be of practical importance for the development of integrated pest management systems. Electronic supplementary material Supplementary material to this paper is available in electronic form at and accessible for authorised users.