Male-Produced Sex Attractant Pheromone of the Green Stink Bug, Acrosternum hilare (Say)

Sexually mature virgin adult males of the green stink bug, Acrosternum hilare attracted sexually mature virgin adult females in laboratory bioassays using a vertical Y-tube. There was no indication that males attracted other males, or that females attracted either sex. These results suggested that A. hilare males produce a sex pheromone. Extracts of odors collected from sexually mature males contained compounds that were not present in extracts from females or sexually immature males. (4S)-Cis-(Z)-bisabolene epoxide ((4S)-cis-Z-BAE) was the major sex-specific component of the extract. The crude extract was attractive to female A. hilare, but when separated into four fractions, only the portion containing (4S)-cis-Z-BAE and the minor component (4S)-trans-Z-BAE was attractive to females. This fraction was as attractive as the crude extract, suggesting that the former contained all the pheromone components. Neither synthetic (4S)-cis-Z-BAE nor (4S)-trans-Z-BAE alone was attractive to females, but a 95:5 cis:trans blend, mimicing the ratio naturally produced by males, was attractive to females in Y-tube bioassays. Bioassays in a field cage showed that significantly more A. hilare females were attracted to cotton string lures treated with 1 mg of a 95:5 blend of (4S)-cis-Z-BAE and (4S)-trans-Z-BAE placed inside a bouquet of alfalfa than to an alfalfa bouquet containing a pentane-treated control. In field cage studies, attraction of females was greatest during the late afternoon and evening hours, and female A. hilare approached the synthetic pheromone source almost exclusively by walking.     

Behavioral Evidence for Olfactory-Based Location of Honeybee Colonies by the Scarab <Emphasis Type="Italic">Oplostomus haroldi</Emphasis>

The Afro-tropical scarab Oplostomus haroldi (Witte) is a pest of honeybees in East Africa with little information available on its chemical ecology. Recently, we identified a female-produced contact sex pheromone, (Z)-9-pentacosene, from the cuticular lipids that attracted males. Here, we investigated the kairomonal basis of host location in O. haroldi. We used coupled gas chromatography/electroantennographic detection (GC/EAD) and GC/mass spectrometry to identify antennally-active compounds from volatiles collected from honeybee colonies. Antennae of both sexes of the beetle consistently detected seven components, which were identified as 3-hydroxy-2-butanone, 2,3-butanediol, butyl acetate, isopentyl acetate, butyl butyrate, hexyl acetate, and methyl benzoate. In olfactometer bioassays, both sexes responded to the full seven-component synthetic blend over solvent controls, but chose honeybee colony odors over the blend. These findings suggest that the seven compounds are components of a kairomone from honeybee colonies used by O. haroldi.     

Female Sex Pheromone in Trails of the Minute Pirate Bug, <Emphasis Type="Italic">Orius minutus</Emphasis> (L)

Orius minutus (L.) (Heteroptera: Anthocoridae) is a natural enemy of agricultural pests such as thrips, aphids, and various newly hatched insect juveniles. In this study, we conducted 1) behavioral assays for evidence of contact sex pheromone activity in trails of O. minutus, and 2) chemical analysis to identify the essential chemical components of the trails. Males showed arrestment to trails of mature virgin females but not to trails from either conspecific nymphs or immature females. Females also showed arrestment to trails from conspecific males, although the response was weaker than that exhibited by males. The activity of female trails lasted for at least 46 h after deposition. Males showed a response irrespective of mating experience. Following confirmation that a contact sex pheromone was present in the trails of female O. minutus, we used a bioassay-driven approach to isolate the active chemicals. After fractionation on silica gel, the n-hexane fraction was found to be biologically active to males. A major compound in the active fraction was (Z)-9-nonacosene; this compound was found only in trail extracts of mature virgin females. Synthetic (Z)-9-nonacosene arrested O. minutus males, indicating that it is the major active component of the contact sex pheromone in the trails of female O. minutus.     

Chemical and behavioral analyses of volatile sex pheromone components released by callingHeliothis virescens (F.) females (Lepidoptera: Noctuidae)

Gas chromatographic and mass spectral analyses were conducted on pheromone gland extracts, volatiles collected from excised pheromone glands, and volatiles collected from calling females. In addition to tetradecanal, (Z)-9-tetradecenal, hexadecanal, (Z)-7-hexadecenal, (Z)-9-hexadecenal, and (Z)-11-hexadecenal, four other compounds, tetradecanol, (Z)-9-tetradecenol, hexadecanol, and (Z)-11-hexadecenol, were also identified from gland extracts. Only the six aldehyde components were found in gland and female volatile collections. The mean percentage of components identified from volatiles collected from calling females was 13.0% tetradecanal, 18.1% (Z)-9-tetradecenal, 7.3% hexadecanal, 0.6% (Z)-7-hexadecenal, 1.0% (Z)-9-hexadecenal, and 60.0% (Z)-11-hexadecenal. Bioassays using rubber septa formulated to release the female volatile blend indicated that all six aldehyde components play major roles in close-range male reproductive behavior. Deletion of (Z)-9-hexadecenal from the six-component blend reduced the number of copulation attempts while (Z)-7-hexadecenal exerted subtle effects on all close range behaviors. Tetradecanal affected the number of times males reorient from close range. Deletion of hexadecanal from the six-component blend resulted in a significant reduction in the number of times males landed. Comparison of the six-component synthetic blend (released at somewhat less than 1 female equivalent per hour) with calling females indicated that the six-component blend was indistinguishable from the females in inducing all of the behaviors monitored.     

Female-produced sexual pheromone ofSceliodes cordalis (Lepidoptera: Pyralidae)

(E)-11-Hexadecen-1-yl acetate and (E)-11-hexadecen-1-ol were identified in extracts from the abdominal pheromone gland of femaleSceliodes cordalis and in a 1∶1 ratio acted as a potent field attractant for males. Sustained upwind flight by males to this mixture in a wind tunnel confirmed the identity of these compounds as major components of the natural sex pheromone of this species. The synthetic pheromone was used to define the annual limits of male flight activity. In the presence of 1–10 μg of pheromone per liter of air, the mating rate of laboratory populations was halved. TheZ isomers of both pheromone components decreased the numbers of males captured in traps baited with virgin females in the field and inhibited upwind flight in the wind tunnel. The attraction of males ofMnesictena flavidalis to virgin females ofS. cordalis and synthetic mixtures was demonstrated to be due to the acetate component alone. MaleEudonia sp. nrlinealis were captured by (Z)-11-hexadecen-1-yl acetate.     

Response of Egg Parasitoid Telenomus busseolae to Sex Pheromone of Sesamia nonagrioides

The olfactory cues involved in the host-finding behavior of Telenomus busseolae Gahan, a solitary egg parasitoid of the corn stalk borer, Sesamia nonagrioides (Lefebvre), were studied. The female wasp was attracted to odors from calling virgin females of S. nonagrioides in a Y-tube olfactometer. No response was elicited by noncalling virgin female moths and/or mated female moths. A four-component commercially available sex pheromone of the corn borer was also tested, as were the individual components of the mixture. T. busseolae respond to the whole blend [(Z)-11-hexadecenyl acetate, (Z)-11-hexadecenol, (Z)-11-hexadecenal, and dodecyl acetate in the ratio of 8.5:1:1:2]. Z11–16:OH was the only compound that elicited no significant activity. These results suggest that the sex pheromone released by the host female S. nonagrioides is used by T. busseolae as an indirect cue to locate egg masses of this host.     

Identification of Sex Pheromone Components of Blueberry Spanworm Itame argillacearia (Lepidoptera: Geometridae)

Blueberry spanworm, Itame argillacearia (Packard), is an important defoliator of lowbush (syn. ‘wild’) blueberry, Vaccinium angustifolium Aiton, in north-eastern North America. The goal of the present study was to identify the female I. argillacearia sex pheromone, which could be used in traps for monitoring or mass-trapping this pest. Gas chromatography/mass spectrometry (GC/MS) and electroantennogram (EAG) recordings of sex pheromone gland extracts, in combination with chemical synthesis, a Y-tube olfactometer study and field experiments confirmed (2R,3S)-2-ethyl-3-((Z,Z)-tridecadi-2,5-enyl) oxirane (hereafter (Z,Z)-(3R,4S)-3,4-epoxy-6,9-heptadecadiene) and (Z,Z,Z)-3,6,9-heptadecatriene as female-produced sex pheromone components. (Z,Z)-(3R,4S)-3,4-Epoxy-6,9-heptadecadiene elicited a response from male I. argillacearia antennae during EAG recording, and in the Y-tube olfactometer tests males did not discriminate between a live female and (Z,Z)-(3R,4S)-3,4-epoxy-6,9-heptadecadiene. Field-trapping experiments showed that a blend of (Z,Z)-(3R,4S)-3,4-epoxy-6,9-heptadecadiene and (Z,Z,Z)-3,6,9-heptadecatriene was more attractive to male moths than (Z,Z)-(3R,4S)-3,4-epoxy-6,9-heptadecadiene alone.     

Unsaturated Cuticular Hydrocarbons Enhance Responses to Sex Pheromone in Spruce Budworm, <Emphasis Type="Italic">Choristoneura fumiferana</Emphasis>

The primary sex pheromone components of the female spruce budworm, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae), are (E)- and (Z)-11-tetradecenal, produced in 95:5 ratio. However, male flight responses to calling females in a wind tunnel were faster and maintained longer than responses to any synthetic aldehyde blend. Analyses of cuticular extracts from spruce budworm adults revealed series of n-alkanes and n-monoalkenes with predominantly odd numbers of carbon atoms from C₂₃- C₂₉ in both sexes. (Z,Z,Z)-3,6,9-tricosatriene and (Z,Z,Z)-3,6,9-pentacosatriene were identified only in cuticular extracts from females. Pheromonally naïve males showed wing fanning and circling responses to forewing scales from females but not to scales from males. Males also exhibited the same strong responses to scales excised from pharate females, indicating that the pheromone components are produced by females prior to emergence. (Z)-11-hexadecenal and (Z)-5-tricosene enhanced male responses to the primary sex pheromone aldehydes in wind tunnel bioassays, including higher proportions of in-flight and copulatory responses by males and increased time on the source. Addition of (Z,Z,Z)-3,6,9-tricosatriene to the 95/5 blend of (E)- and (Z)-11-tetradecenal released close-range copulatory responses including abdomen curling on treated septa. We propose that the sex pheromone blend of C. fumiferana is composed of the 95/5 blend of (E)- and (Z)-11-tetradecenal as primary components, with (Z)-11-hexadecenal, (Z)-5-tricosene and (Z,Z,Z)-3,6,9-tricosatriene fulfilling secondary roles in orientation and close-range courtship.     

Sex Pheromone of the Mirid Bug Phytocoris relativus

The sex attractant pheromone produced by adult females of the mirid bug Phytocoris retativus has been identified as a 2:1 blend of hexyl acetate with (E)-2-octenyl butyrate. The pheromone is stage-, sex-, and species-specific, attracting only adult male P. relativus. Hexyl acetate was identified in aeration extracts from both sexes, while (E)-2-octenyl butyrate was produced only by females. Both males and females also produced hexyl butyrate and octyl acetate, while only females produced (E)-2-hexenyl and octenyl acetates, and (Z)-3-octenyl acetate. The function(s) of these chemicals were not determined. Attraction of males increased with dose, with doses of 0.1 to 33 mg loaded on grey rubber septa. Attractiveness of rubber septum lures decreased quickly with age due to the volatility of the two pheromone components.     

(Z)-5-tetradecen-1-ol: A secondary pheromone of the yellowheaded spruce sawfly,and its relationship to (Z)-10-nonadecenal

The yellowheaded spruce sawfly,Pikonema alaskensis (Rohwer), was known to possess a potent secondary pheromone with the polarity of an alcohol, based on earlier studies with Florisil fractions. Purification of the 25% ether-hexane Florisil fraction (polarity as with alcohols) and the hydrolyzed 5% ether-hexane fraction (polarity as with esters) from 50,000 females yielded a total of ca 3μg of an active compound identified as (Z)-5-tetradecen-1-ol (Z5–14∶ OH). When added to 100 ng of (Z)-10-nonadecenal (Z10–19∶Al), which behaves as the primary pheromone in this sawfly, 0.5 ng of syntheticZ5–14∶ OH caused an 8.8-fold increase in the greenhouse bioassay response, compared toZ10–19∶Al alone.E5–14∶ OH caused a 2.8-fold increase. Only the combination ofZ5–14∶ OH andZ10–19∶ Al consistently elicited mating attempts among males. When Hercon® formulations ofZ5–14∶OH andZ10–19∶ Al were used together to bait traps, catches were up to four times higher than for theZ10–19∶ Al alone, but this increase was seen only after emergence and mating activity in the field population were virtually complete. TheZ5–14∶ OH was inactive alone, and at higher levels it depressed trap catches toZ10–19∶ Al. The Hercon formulations ofZ5–14∶ 0H andZ10–19∶Al together were as attractive as virgin females.Z10–19∶Al alone and the (Z,Z)-9,19 hydrocarbon dienes (found in all females and able to oxidize in air to produceZ10–19∶Al) were similar to mated females. ThusZ5–14∶:OH accounted for the difference in attractiveness between virgin and mated females.     

Identification of new sex pheromone components inTrichoplusia ni,predicted from biosynthetic precursors

In addition to the previously identified components (Z)-7-dodecenyl acetate and dodecyl acetate, sex pheromone glands ofTrichoplusia ni release (Z)-5-dodecenyl acetate, 11-dodecenyl acetate, (Z)-7-tetradecenyl acetate, and (Z)-9-tetradecenyl acetate. Bioassays in a flight tunnel showed that a synthetic blend of these six compounds elicited complete flights to the source from 95% of the males tested and elicited hairpenciling responses at the end of the flights from 88% of the males tested. This blend was not significantly different from intact pheromone glands, which elicited complete flights to the source from 98% of the males tested and hairpenciling responses from 91% of the males tested. In contrast, the previously identified two-component blend elicited significantly fewer complete flights to the source (33%) and did not elicit hairpenciling responses from any of the males tested. The search for additional sex pheromone components was prompted by our previous identification of unusual fatty acyl moieties in the gland that seemed to be possible biosynthetic intermediates.     

Optimization of Pheromone Dispensers for Diamondback Moth Plutella xylostella

We have investigated the effects of pheromone dispenser design, pheromone release rate, and the products of Z11–16:Ald decomposition on the attractiveness of the pheromone blend (Z)-11-hexadecenyl acetate, (Z)-11-hexadecenal, and (Z)-11-hexadecen-1-ol) in traps to Plutella xylostella males. Rubber minidispensers (K-50) were shown to have an active exposure time of at least two months and in delta traps to be capable of monitoring a population of P. xylostella throughout the summer in Estonia. Pheromone release rates between 8 and 17 ng/hr are recommended for maximum trap catches. The attractive blend contained 15–35% of Z11–16:Ac. Decomposition products of Z11–16:Ald inhibited the activity of the pheromone blend when more than 50% of the aldehyde had decomposed.     

Formate Analogs as Antagonists of the Sex Pheromone of the Honeydew Moth, Cryptoblabes gnidiella: Electrophysiological, Behavioral and Field Evidence

Cryptoblabes gnidiella Milliére (Lepidoptera: Pyralidae) is an economically important exotic pest of vineyards in Southern Brazil and Uruguay. The sex pheromone of C. gnidiella was identified as a mixture of (Z)-11-hexadecenal and (Z)-13-octadecenal, and has been used to monitor populations of this pest in Israel. The development of mating disruption for this species may be hampered by the chemical instability of the natural pheromone components. Therefore, studies on more stable pheromone analogs may provide tools for a control strategy based on behavior-modifying chemicals. We report here the electrophysiological and behavioral responses of C. gnidiella males to (Z)-9-tetradecenyl formate and (Z)-11-hexadecenyl formate, structural analogs of the pheromone components. In gas chromatography-electroantennogram detection (GC-EAD) studies, both analogs elicited responses from C. gnidiella male antennae. Pre-exposure to the formates did not affect the subsequent EAD responses to the natural pheromone components. The formates acted as pheromone antagonists in wind tunnel tests, inhibiting the responses of males toward both synthetic pheromone and calling females. In the field, captures of males in pheromone-baited traps decreased, in a dose-response pattern, when different amount of formates were added to the pheromone. These pheromone antagonists, thus, are potentially useful as mating disruptants for C. gnidiella in commercial vineyards.     

EFFECT OF PBAN ON PHEROMONE PRODUCTION BY MATED <Emphasis Type="Italic">Heliothis virescens</Emphasis> AND <Emphasis Type="Italic">Heliothis subflexa</Emphasis> FEMALES

Mated female Heliothis virescens and H. subflexa were induced to produce sex pheromone during the photophase by injection of pheromone biosynthesis activating neuropeptide (PBAN). When injected with 1 pmol Hez-PBAN, the total amount of pheromone that could be extracted from glands of mated females during the photophase was similar to that extracted from virgin females in the scotophase. The PBAN-induced profile of pheromone components was compared between mated, PBAN-injected females and virgin females during spring and fall. Virgin females exhibited some differences in the relative composition of the pheromone blend between spring and fall, but no such temporal differences were detected in PBAN-injected, mated females. Because the temporal variation in pheromone blend composition was greater for virgin females than for PBAN-injected females, PBAN can be used to determine a females native pheromone phenotype. This procedure has the advantages that pheromone glands can be extracted during the photophase, from mated females that have already oviposited.     

Variability in Pheromone Communication Among Different Haplotype Populations of <Emphasis Type="Italic">Busseola fusca</Emphasis>

The relationship between pheromone composition and mitochondrial haplotype clades was investigated by coupling DNA analyses with pheromone identification and male mate searching behavior among different geographic populations of Busseola fusca. The within-population variations in pheromone blend were as great as those observed between geographic populations, suggesting that the female sex pheromone blend was not the basis of reproductive isolation between the geographic clades. Furthermore, while data from wind tunnel experiments demonstrated that most of the tested males were sensitive to small variations in pheromone mixture, there was considerable within-population variability in the observed response. The study identified a new pheromone component, (Z)-11-hexadecen-1-yl acetate, which when added to the currently used three-component synthetic blend resulted in significantly higher traps catches. The new recommended blend for monitoring flight phenology and for timing control measures for optimal efficacy of B. fusca is (Z)-11-tetradecen-1-yl acetate (62%), (E)-11-tetradecen-1-yl acetate (15%), (Z)-9-tetradecen-1-yl acetate (13%), and (Z)-11-hexadecen-1-yl acetate (10%).     

Identification of an attractant for the caneborerSesamia grisescens walker (Lepidoptera: Noctuidae)

The composition of the sex pheromone ofSesamia grisescens was investigated using gas chromatography, electroantennograms, and field trapping. (Z)-11-Hexadecenyl acetate and (Z)-11-hexadecenol were identified in field tests as the major attractants. Trapping trials identified a 3:2 blend of these compounds as the most effective bait. Gas chromatography indicated the presence of hexadecyl acetate. (Z)-9-hexadecenyl acetate, (Z)-9-hexadecenol, and (E)-11-hexadecenyl acetate in the pheromone gland, but these compounds had no significant effect on trap catches when added to the major components. Traps baited with the major components in a 1:1 ratio caught more male moths than traps baited with virgin females.     

Role of sex pheromone components in behavioral reproductive isolation betweenAutographa gamma (L.) and eitherTrichoplusia ni (Hübner) ORChrysodeixis chalcites (Esp.) (Lepidoptera: Noctuidae: Plusiinae)

The composition of theAutographa gamma sex pheromone was reexamined and only (Z)-7-dodecenyl acetate and (Z)-7-dodecenol were identified by capillary GC, GC-MS, and dimethyl disulfide derivatization and subsequent GC-MS analysis. The fatty acid content of the pheromone glands was also studied, and a series of saturated and unsaturated acids was identified. However, most of the related pheromonal compounds were not detected. The male response to the pheromone components was studied in a flight tunnel and compared with the response to calling females. The best synthetic baits evoked a response similar to that observed to the virgin females, but males spent significantly more time at calling females than at the synthetic baits. The preferred synthetic baits consisted of (Z)-7-dodecenyl acetate alone or of a blend with 5% (Z)-7-dodecenol. Increasing the relative amount of the alcohol caused a gradual reduction in male response, particularly in the last steps of the courtship sequence. The addition of the minor sex pheromone components of the sympatric Plusiinae species,Trichoplusia ni andChrysodeixis chalcites, to theA. gamma pheromone was also investigated in the flight tunnel. Some of these components exhibited a significantly antagonistic effect on theA. gamma male courtship behavior. The most potent antagonists were (Z)-5-dodecenyl acetate and (Z)-9-tetradecenyl acetate. The response ofA. gamma andT. ni males to conspecific and heterospecific females was also compared in the flight tunnel. WhereasA. gamma males were attracted only to their conspecific females, a small percentage ofT. ni males were also attracted toA. gamma females and 11% performed the whole courtship sequence.Contribution from the Agricultural Research Organization (ARO), No. 3459-E, 1992 series.     

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.     

Particular Levels of Odors Released by Virgin Females Attract Conspecific Males of the Funnel-Web Spider <Emphasis Type="Italic">Allagelena difficilis</Emphasis>

Female-released chemical signals are crucial clues for mate-searching males to locate and gain sexual receptivity of conspecific females. Abundant behavioral evidence indicates that female spiders release sex pheromones to guide mate-searching behavior of conspecific mature males. However, the chemical nature of spider pheromones is poorly understood. Females of the funnel-web spider, Allagelena difficilis, employ sit-and-wait tactics for mating. Field observations indicate that males leave their retreats to search for potential mates during the breeding season. Therefore, we investigated whether virgin females release a sex attractant to conspecific males and then explored the chemical nature of the female pheromone. Four fatty acids extracted from the female bodies (palmitic acid, linoleic acid, cis-vaccenic acid and stearic acid) constitute a multiple-component sex attractant to conspecific males in A. difficilis. Unexpectedly, mated females also produce the same fatty acids, but at trace levels. Two-choice experiments showed that males were significantly attracted by the blend of the four fatty acids in appropriate concentrations while avoiding the blend consisting of the same acids at very low concentrations, suggesting that mate-searching males are able to discriminate virgin females from mated females by the quantities of female-specific fatty acids in the funnel-web spider A. difficilis.     

Attractiveness of a Four-component Pheromone Blend to Male Navel Orangeworm Moths

The attractiveness to male navel orangeworm moth, Amyelois transitella, of various combinations of a four-component pheromone blend was measured in wind-tunnel bioassays. Upwind flight along the pheromone plume and landing on the odor source required the simultaneous presence of two components, (11Z,13Z)-hexadecadienal and (3Z,6Z,9Z,12Z,15Z)-tricosapentaene, and the addition of either (11Z,13Z)-hexadecadien-1-ol or (11Z,13E)-hexadecadien-1-ol. A mixture of all four components produced the highest levels of rapid source location and source contact. In wind-tunnel assays, males did not seem to distinguish among a wide range of ratios of any of the three components added to (11Z,13Z)-hexadecadienal. Dosages of 10 and 100 ng of the 4-component blend produced higher levels of source location than dosages of 1 and 1,000 ng.