Male Sex Pheromonal Components Derived from Methyl Eugenol in the Hemolymph of the Fruit Fly Bactrocera papayae

Pharmacophagy of methyl eugenol (ME)--a highly potent male attractant, by Bactrocera papayae results in the hydroxylation of ME to sex pheromonal components, 2-ally-4,5-dimethoxyphenol (DMP) and (E)-coniferyl alcohol (CF). These compounds, which are also male attractants, are then sequestered and stored in the rectal gland prior to their release during courtship at dusk. Chemical analyses of the digestive tract (excluding the crop and rectal gland) showed the absence of the sex pheromonal components and their precursor, ME. However, B. papayae males were attracted to and fed on the ME-fed male hemolymph extracts but not on hemolymph extracts of ME-deprived males. After thin layer chromatography in a hexane:ethyl acetate solvent system, flies were attracted to and fed on the original point on the TLC plate where the hemolymph extract had been spotted, suggesting that the pheromone components were bound in polar complexes. Chemical analyses of the ME-fed male hemolymph and crop extracts revealed the presence of the sex pheromonal components. The presence of the ME-derived pheromonal components and the absence of ME in the hemolymph suggest that the hemolymph is involved in the transportation of sex pheromonal components from the crop to the rectal gland.     

Attraction of Female Bactrocera papayae to Sex Pheromone Components with Two Different Release Devices

We determined female attraction to coniferyl alcohol (CF) and 2–allyl-4,5–dimethoxyphenol (DMP) dispensed individually and in combinations from a syringe driver (SD) or a rubber septum (RS), at different concentrations and in combination at different ratios. While female attraction to both compounds varied at different concentrations, females were more attracted to CF than to DMP. Combination of both compounds showed that DMP enhanced the attractiveness of CF only when CF was at suboptimal concentrations. Both compounds attracted most females at a release rate of 0.5 g/15 min. In addition, decreasing light intensity showed an interaction with the concentration of the compound used by enhancing the attractiveness of DMP and CF to females. Results also demonstrated that SD, being a controlled release device, was more satisfactory for dispensing CF and DMP.     

Evidence of Natural Hybridization Between Two Sympatric Sibling Species of <Emphasis Type="Italic">Bactrocera dorsalis</Emphasis> Complex Based on Pheromone Analysis

Bactrocera carambolae and B. papayae are major fruit fly pests and sympatric sibling species of the B. dorsalis complex. They possess distinct differences in male pheromonal components. In the 1990s, wild Bactrocera fruit flies with morphological traits intermediate between those of B. carambolae and B. papayae were often captured in traps baited with methyl eugenol (ME). Chemical analyses of rectal glands of ME-fed males revealed that the laboratory F₁, F₂, and backcross hybrids possessed ME-derived sex pheromonal components ranging from that typical of B. papayae to that of B. carambolae without any specific trend, which included a combination of pheromonal components from both parental species within an individual hybrid. ME-fed hybrids without any ME-derived pheromonal components were also detected. Further chemical analysis of rectal glands from wild Bactrocera males, after ME feeding in the laboratory, showed a combination of pheromonal components similar to that found in the ME-fed, laboratory-bred hybrids. These findings present circumstantial evidence for the occurrence of a natural hybrid of the two Bactrocera species.     

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.     

Pheromone Components from Body Scales of Female <Emphasis Type="Italic">Anarsia lineatella</Emphasis> Induce Contacts by Conspecific Males

Pheromonal communication of adult peach twig borers, Anarsia lineatella Zeller (Lepidoptera: Gelechiidae), was reinvestigated based on recent findings that virgin female-baited traps were more attractive to mate-seeking males than a two-component synthetic sex pheromone consisting of (E)-5-decen-1-yl acetate (1000 μg) and (E)-5-decen-1-ol (100 μg), suggesting that females use additional pheromone components. Hypothesizing that these additional components may be released from body parts other than abdominal sex pheromone glands, we extracted female body scales and analyzed aliquots by coupled gas chromatographic–electroantennographic detection (GC-EAD) and GC–mass spectrometry. Eight straight-chain and four methylated aliphatic hydrocarbons, as well as two acetates, all elicited responses from excised male antennae. In laboratory experiments with synthetic candidate pheromone components, a combination of octadecyl acetate, (R)-11-methyltricosane, and (S)-11-methyltricosane in the presence of gland-derived sex pheromone components were shown to elicit contact of female decoys by males. However, body pheromone components did not enhance attractiveness of sex pheromone components in field trapping experiments, suggesting that they are effective only at close range and that other stimuli are responsible for superior attractiveness of female-baited traps.     

Consumption and Metabolism of 1,2-Dimethoxy-4-(3-Fluoro-2-Propenyl)Benzene, a Fluorine Analog of Methyl Eugenol, in the Oriental Fruit Fly Bactrocera dorsalis (Hendel)

Methyl eugenol (ME) is a natural phenylpropanoid highly attractive to oriental fruit fly Bactrocera dorsalis (Hendel) males. The flies eagerly feed on ME and produce hydroxylated metabolites with both pheromonal and allomonal functions. Side-chain metabolic activation of ME has long been recognized as a primary reason for hepatocarcinogenicity of this compound on rodents. In an attempt to develop a safer alternative to ME for fruit fly management, we developed a fluorine analog 1,2-dimethoxy-4-(3-fluoro-2-propenyl)benzene (I), which, in earlier field tests, was as active to the oriental fruit fly as ME. Now we report that B. dorsalis males are not only attracted to, but also eagerly consume (up to ∼1 mg/insect) compound I, thus recognizing this fluorinated benzene as a close kin of the natural ME. The flies metabolized the fluorine analog I in a similar fashion producing mostly two hydroxylated products, 2-(3-fluoro-2-propenyl)-4,5-dimethoxyphenol (II) and (E)-coniferyl alcohol (III), which they stored in rectal glands. However, the introduction of the fluorine atom at the terminal carbon atom of the double bond favors the ring hydroxylation over a side-chain metabolic oxidation pathway, by which coniferyl alcohol is produced. It also appears that fluorination overall impedes the metabolism: at high feed rate (10 μl per 10 males), the flies consumed in total more fluorine analog I than ME but were unable to metabolize it as efficiently as ME.     

Minor and Intermediate Components Enhance Attraction of Female Mediterranean Fruit Flies to Natural Male Odor Pheromone and Its Synthetic Major Components

The attraction of virgin female medflies to either the natural pheromonal odor of calling males or its synthetic major components was enhanced by both intermediate and minor pheromonal components in multiple choice discrimination tests. The modification of the standard Gow rotating-trap-array, cage olfactometer to allow a single source of natural pheromonal odor to be delivered equally and simultaneously to a number of traps greatly increased trapping efficacy (64% capture rate) and ability to resolve odor preference discrimination by female flies. In olfactometer cage bioassays, responding female medflies expressed preferences in attraction to male odor augmented with either synthetic intermediate or minor components over male odor alone. In dual-choice flight-tunnel bioassays, the minor blend enhanced the attractiveness of both the natural male odor and its synthetic major components. Moreover, the minor blend, when presented together with the synthetic major components, comprised an artificial pheromonal lure competitive for the first time with the natural male odor in attraction of virgin female medflies.     

Identification and Field Evaluation of Components of Female Sex Pheromone of Millet Stem Borer, Coniesta ignefusalis

Five active compounds were detected during analyses of ovipositor washings and effluvia from virgin female Coniesta ignefusalis moths by gas chromatography (GC) linked to electroantennographic (EAG) recording from a male moth. These were identified as (Z)-7-dodecen-1-ol (Z7–12:OH), (Z)-5-decen-1-ol (Z5–10:OH), (Z)-7-dodecenal (Z7–12:Ald), (Z)-7-dodecenyl acetate (Z7–12:Ac), and (Z)-9-tetradecen-1-ol (Z9–14:OH) by comparison of their GC retention times, mass spectra, and EAG activities with those of synthetic standards. Laboratory tests of dispensers for these compounds showed that release rates from polyethylene vials increased to relatively uniform values after three to four days, but release from septa was very rapid and nonuniform and decreased to low levels after two to three days. Trapping tests in Niger showed that the major component, Z7–12:OH, and two of the minor components, Z5–10:OH and Z7–12:Ald, were essential for attraction of male C. ignefusalis moths. The most attractive blend contained these three components in a 100:5:3.3 ratio in a polyethylene vial, which emitted the components in similar proportions to those produced by the female C. ignefusalis moth. Water traps baited with this blend containing 1 mg of Z7–12:OH caught more male C. ignefusalis moths than traps baited with newly emerged female moths. Addition of up to 10% of the corresponding E isomers of the pheromone components had no effect on catches, but addition of the other two minor components detected, Z7–12:Ac and/or Z9–14:OH, to the attractive blend at naturally occurring levels caused significant reductions in trap catch.     

Attraction of Male European Tarnished Plant Bug, <Emphasis Type="Italic">Lygus rugulipennis</Emphasis> to Components of the Female Sex Pheromone in the Field

Previous work showed that females of the European tarnished plant bug, Lygus rugulipennis Poppius (Heteroptera: Miridae), produced three chemicals, hexyl butyrate, (E)-2-hexenyl butyrate, and (E)-4-oxo-2-hexenal, and that these were suspected to be components of the female sex pheromone. In field experiments, traps baited with blends of these chemicals dispensed from polyethylene vials and sachets failed to catch significant numbers of males. Here, we report more recent field experiments in which the chemicals were released from glass microcapillary tubes. A blend of hexyl butyrate and (E)-4-oxo-2-hexenal was significantly attractive to male L. rugulipennis. In addition, whereas the mixture of all three components attracted fewer L. rugulipennis males, this tertiary blend captured significantly greater numbers of males of the congeneric species Lygus pratensis than the binary mixture. The possible reasons for the success of the microcapillaries compared with other dispensers are discussed.     

Evaluation of the Major Female Eurytoma amygdali Sex Pheromone Components, (Z,Z)-6,9-Tricosadiene and (Z,Z)-6,9-Pentacosadiene for Male Attraction in Field Tests

We evaluated the attraction of male almond seed wasp Eurytoma amygdali to the synthetic alkadienes (Z,Z)-6,9-tricosadiene and (Z,Z)-6,9-pentacosadiene and their blend in almond orchards using baited rubber septa attached to cardboard rectangular adhesive traps. The two alkadienes were recently isolated from virgin female whole body extracts and SPME collected volatiles. The alkenes (Z)-9-tricosene, (Z)-9-pentacosene, and (Z)-9-heptacosene, present in female extracts, were also added to the blend of the alkadienes and tested. The alkadienes tested individually attracted males when the traps were baited with doses ranging from 10 to 30 mg/trap. The maximum number of males was attracted to traps baited with 10 mg of a (Z,Z)-6,9-C(23:2):(Z,Z)-6,9-C(25:2) blend at a ratio of 7:3. Results with the three alkenes added to the blend were inconclusive because of low populations. The present study on E. amygdali is the first one reporting attraction of males to synthetic sex pheromone components in field trials for a Eurytomidae species. The synthetic alkadienes blend offers the potential to develop an effective system for monitoring populations of the almond seed wasp in almond orchards.     

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.     

Ring-Fluorinated Analog of Methyl Eugenol: Attractiveness to and Metabolism in the Oriental Fruit Fly, <Emphasis Type="Italic">Bactrocera Dorsalis</Emphasis> (Hendel)

Oriental fruit fly, Bactrocera dorsalis (Hendel), males are highly attracted to the natural phenylpropanoid methyl eugenol (ME). They compulsively feed on ME and metabolize it to ring and side-chain hydroxylated compounds that have both pheromonal and allomonal functions. Side-chain metabolic activation of ME leading to (E)-coniferyl alcohol has long been recognized as a primary reason for hepatocarcinogenicity of this compound in rodents. Earlier, we demonstrated that introduction of a fluorine atom at the terminal carbon of the ME side chain significantly depressed metabolism and specifically reduced formation of coniferyl alcohol but had little effect on field attractiveness to B. dorsalis. In the current paper, we demonstrate that fluorination of ME at the 4 position of the aromatic ring blocks metabolic ring-hydroxylation but overall enhances side-chain metabolism by increasing production of fluorinated (E)-coniferyl alcohol. In laboratory experiments, oriental fruit fly males were attracted to and readily consumed 1,2-dimethoxy-4-fluoro-5-(2-propenyl)benzene (I) at rates similar to ME but metabolized it faster. Flies that consumed the fluorine analog were as healthy post feeding as ones fed on methyl eugenol. In field trials, the fluorine analog I was ∼50% less attractive to male B. dorsalis than ME.

Identification of Epoxyhenicosadiene and Novel Diepoxy Derivatives as Sex Pheromone Components of the Clear-Winged Tussock Moth Perina nuda

Four EAG-active components (A–D) were found in the solvent extract of virgin females of the clear-winged tussock moth, Perina nuda. The most abundant component (B, ca. 250 ng/female) was identified as (3Z,6S,7R,9Z)-6,7-epoxyhenicosa-3,9-diene by GC-MS analyses of the extract, chemical derivatization, and comparative chiral HPLC. Minor components also elucidated were (3Z,9Z)-cis-6,7-epoxyicosa-3,9-diene, (A); (3R,4S,6S,7R,9Z)-3,4-6,7-diepoxyhenicos-9-ene, (C); and its 3S,4R,6S,7R isomer, (D); with amounts of 0.4, 5, and 8 ngt/female, respectively. Component B showed weak attractiveness to male moths in the field. The attractiveness was significantly enhanced by addition of component(s) C and/or D. No males were captured with either the antipode of component B or its mixtures with the minor components. In this field test, noctuid Hypocala rostrata males were also attracted with the synthetic P. nuda pheromone.     

Identification of Two Sex Pheromone Components of the Potato Aphid, Macrosiphum euphorbiae (Thomas)

Females of the potato aphid Macrosiphum euphorbiae exhibit typical calling behavior, with virgin female oviparae raising their back legs off the substrate to release sex pheromone from glands on the tibia. Airborne collections from calling oviparae were analyzed by GC and GC-MS to determine if, like the majority of aphids examined to date, they produced (1R,4aS,7S,7aR)-nepetalactol (1) and (4aS,7S,7aR)-nepetalactone (2). Both components were present and produced in ratios that varied with age from 4:1 to 2:1. The relative stereochemical configurations of these components were determined by GC-coinjection of the aphid-derived sample with synthetic standards on both HP-1 and DB-Wax GC columns. The absolute stereochemical configuration of the nepetalactol (determined from approximately 15 microg of material in an air entrainment sample) was determined as (1R,4aS,7S,7aR)-1 by derivatization of the aphid sample with (S)-(+)-alpha-methoxy-alpha-(trifluoromethyl)phenylacetyl chloride (Mosher's acid chloride) to generate a diastereoisomer that was compared to synthetic samples by NMR spectroscopy and GC. In bioassays in the wind tunnel, M. euphorbiae males responded to potato plants with oviparae but not to unattacked plants or those infested with parthenogenetically reproducing apterae. In no-choice laboratory bioassays, the same level of male response was observed to virgins and to the 3:1-5:1 synthetic blends of nepetalactol (1):nepetalactone (2). However, the time taken to reach the source was significantly less to virgin females than to the synthetic pheromone blends. In all cases, males walked rather than flew to the source. Males showed lower responses to a 1:1 synthetic mixture and did not respond to either of the components when presented alone. Under field conditions, few M. euphorbiae males were captured in traps baited with different ratios of the synthetic pheromone. Possible reasons for the different responses under laboratory and field conditions are discussed.     

Decadienoates: Sex Pheromone Components of Nettle Caterpillars Darna trima and D. bradleyi

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.     

Subtleties in Perception and Discrimination by Cabbage Looper Moths, Trichoplusia ni, of the two 14-carbon Acetate Sex Pheromone Components

Three compounds that are emitted by virgin female cabbage looper moths, Trichoplusia ni, (Z)-7-dodecenyl acetate (Z7–12:Ac), (Z)-7-tetradecenyl acetate (Z7–14:Ac), and (Z)-9-tetradecenyl acetate (Z9–14:Ac), are detected by antennal olfactory receptor neurons specialized to detect sex pheromone components. The principal evidence signifying that either or both of Z7–14:Ac and Z9–14:Ac have an effect on male behavior comes from an observed reduction in the numbers of males trapped by Z7–12:Ac paired with a six-component mixture. The evidence conforms to a hypothesis that either or both of these compounds are the basis for discrimination between the two mixtures. However, scant evidence for this hypothesis was obtained in paired-source laboratory wind-tunnel assays, even at airborne concentrations of Z7–14:Ac and Z9–14:Ac that ranged up to 1000× that emitted by a female. Furthermore, there was little evidence from single-source laboratory or field trap assays confirming that Z7–14:Ac and Z9–14:Ac at or above natural stimulus strengths modify the moth's perception of Z7–12:Ac. The data suggest that discrimination of small mixture differences may not be resolvable within the confines of a wind tunnel.     

Chemical, Electrophysiological, and Behavioral Investigations on the Sex Pheromone of Lackey Moth, Malacosoma neustrium

The lackey moth Malacosoma neustrium (L.) (Lepidoptera Lasiocampidae) is a common pest of many forest and cultivated broadleaf trees. Analysis by GC-EAD of gland extracts and female effluvia showed the presence of two active peaks that were characterized as (E,Z)-5,7-dodecadienal (E5,Z7-12:Ald) and (E,Z)-5,7-dodecadienol (E5,Z7-12:OH) according to their GC retention times, mass spectra, and electroantennographic activity. (E,Z)-5,7-dodecadienyl acetate (E5,Z7-12:Ac) was also detected in the gland extracts. The average amounts of E5,Z7-12:Ald, E5,Z7-12:OH, and E5,Z7-12:Ac extracted from an abdominal tip were 113.2 +/- 22.0 ng, 29.9 +/- 6.2 ng, and 11.6 +/- 2.0 ng, respectively. In the effluvia from single females, on the average, 1.9 +/- 0.7 ng/min of aldehyde and 0.3 +/- 0.1 ng/min of alcohol were collected. In wind tunnel tests, male behavioral sequences elicited by E5,Z7-12:Ald alone or in 3:1 and 9:1 blends with the corresponding alcohol were similar to those evoked by one female equivalent of sex pheromone gland extract. Field trapping experiments showed that E5,Z7-12:Ald is essential to attract male moths. On adding E5,Z7-12:OH to E5,Z7-12:Ald in 1:3 and 1:9 ratios, male attraction slightly increased whereas in a 1:1 ratio, the attractiveness of E5,Z7-12:Ald was reduced.     

Attraction of Female Oriental Fruit Fly, Bactrocera dorsalis, to Volatile Semiochemicals from Leaves and Extracts of a Nonhost Plant, Panax (Polyscias guilfoylei) in Laboratory and Olfactometer Assays

Fresh whole leaves and solvent–water leaf extracts of the hedgerow plant panax, Polyscias guilfoylei (Bull), were tested for their attractiveness to male and female Oriental fruit flies, Bactrocera dorsalis, in laboratory flight tunnel and cage olfactometer bioassays. Fresh mature whole panax leaves were found to be attractive to mated female oriental fruit flies in the flight tunnel. Response of males and virgin females was low and in most instances not significantly different from controls. Attraction of mated female flies to the layers resulting from a methylene chloride–water partition or a hexane–water partition of freshly ground leaves using small McPhail traps was greatest in the methylene chloride fraction. When methylene chloride and water layers were tested competitively in a multiple-choice rotating olfactometer, the methylene chloride fraction was more attractive. Tests involving the methylene chloride–water interface (an emulsion of the two partitioned layers) with and without a standard attractant NuLure, showed the emulsion layer to be significantly more attractive than the other fractions or NuLure. In outdoor cage olfactometer assays of methylene chloride and water fractions, activity was greatest in the methylene chloride fraction. The results suggests that volatile semiochemicals from this nonhost plant are attractive to mated female Oriental fruit flies. The results are discussed in relation to the chemical ecology of B. dorsalis and the potential use of this nonhost plant for detection and control of female Oriental fruit flies in the field.     

Comparative Responses of Parasitoids to Synthetic and Plant-Extracted Nepetalactone Component of Aphid Sex Pheromones

The responses of aphid parasitoids to completely synthetic and plant-extracted nepetalactone, a component of aphid sex pheromones, were investigated. In wind tunnel tests, Praon volucre and Aphidius ervi responded equally strongly to both plant-extracted and 99% pure synthetic (4aS,7S,7aR)-nepetalactone. In the field, aphid-infested cereal trap plants were used to test the attractiveness of plant-extracted and synthetic (4aS,7S,7aR)-nepetalactone, as well as the synthetic enantiomer (4aR,7R,7aS)-nepetalactone. There was no significant difference in parasitisation levels by Praon spp. between plants baited with the synthetic or with the plant-extracted 7S isomers. However, the 7R isomer was unattractive alone and rendered the synthetic 7S isomer unattractive when combined to form a 50% blend of the two. It is concluded that the response of aphid parasitoids to nepetalactone is influenced more by enantiomeric purity rather than the possible presence of plant-related contaminants associated with plant extraction. The results are compared with data on male aphid responses to the compounds, which indicate that plant-derived contaminants can reduce attractancy, and the implications for the manipulation of parasitoids in the field are discussed.