Sex attractant of the alfalfa looperAutographa californica and the celery looperAnagrapha falcifera (Lepidoptera: Noctuidae)

In field tests, traps baited with a combination of (Z)-7-dodecen-1-ol acetate (previously proposed to be the sex pheromone ofA. californica) and (Z)-7-dodecen-1-ol formate caught about 100 times as many males as (Z)-7-dodecen-1-ol acetate did alone. Highest catches of males were obtained with traps baited with 0.5 mg of (Z)-7-dodecen-1-ol acetate and 0.1 mg of (Z)-7-dodecen-1-ol formate impregnated on red rubber sleeve stoppers. The celery looper,Anagrapha falcifera, was also caught in traps baited with a combination of these two chemicals.     

Performance criteria and specifications for laminated plastic sex pheromone dispenser forHelicoverpa zea (Lepidoptera: Noctuidae)

Biological and chemical evaluations of a plastic laminate sex pheromone dispenser forHelicoverpa zea (Boddie) were made in central Texas. Based on these evaluations, the following performance criteria and specifications are suggested for a dispenser to be effective for two weeks: (1) 1.27 × 2.54-cm size; (2) 400-m thick orange PVC outer layers; (3) 1.25 mg of a blend of (Z)-11-hexadecenal, (Z)-9-hexadecenal, (Z)-7-hexadecenal, and hexadecanal in a ratio of 87328 formulated in the adhesive reservoir layer; (4) release rate in the range of 0.12-0.33 gJhrJdispenser, as measured in the laboratory at 35°C; and (5) residual pheromone content in the range of 0.55–1.25 mgJdispenser during the period of use.This paper reports the results of research only. Mention of a proprietary product does not constitute an endorsement by the USDA.     

Identification of sex attractant pheromone components of the tussock moth,Euproctis taiwana (Shiraki) (Lepidoptera: Lymantriidae)

Two compounds were isolated and identified from abdominal tips of the female tussock moth,Euproctis taiwana (Shiraki), by a combination of gas chromatography-electroantennographic detection, coupled gas chromatography-mass spectrometric analysis, microreaction, and synthesis. These compounds were (Z)-16-methyl-9-heptadecenyl isobutyrate (74.8%) and 16-methylheptadecyl isobutyrate (25.2%). Their total amount was determined to be ca. 29.8 ng/female. Field bioassays showed that (Z)-16-methyl-9-heptadecenyl isobutyrate is a sex attractant for the male moths. These chemical compounds had not previously been found as the sex pheromone components in the genusEuproctis.     

Identification of a male-produced pheromone ofAnticarsia gemmatalis (Hübner) (Lepidoptera; Noctuidae) attractive to conspecific males

Observations in the laboratory and in the field indicated that maleAnticarsia gemmatalis (Hübner), the velvetbean caterpillar (VBC), are attracted to conspecific courting males. Male VBC subsequently were found to be attracted to extracts of male abdominal tips including the extrudable hairpencils. The active chemical in these extracts was identified as (Z,Z,Z)-3,6,9-heneicosatriene, which is also one of the major components of the female VBC sex pheromone. Male VBC in a wind tunnel and in the field exhibited a bimodal response distribution to a range of ratios of the (Z,Z,Z)-3,6,9-heneicosatriene and (Z,Z,Z)-3,6,9-eicosatriene, with one maximum at the pure heneicosatriene alone and the other at the 6040 female blend. This demonstrates that the male response to the male hairpencil component is distinct from that to the female sex pheromone.This article reports the results of research only. Mention of a proprietary product does not constitute an endorsement or the recommendation for its use by USDA.     

Flight response ofHeliothis subflexa (Gn.) females (Lepidoptera: Noctuidae) to an attractant from groundcherry,Physalis angulata L.

Mated femaleHeliothis subflexa (Gn.) (HS) moths 1–7 days old responded positively in a Plexiglas flight tunnel to an attractant extracted with methanol from fresh whole-leaf washes of groundcherry,Physalis angulata L. Response to the groundcherry extract, as indicated by plume-tracking (i.e., upwind flight toward the odor source) and contact with the chemical dispenser did not change significantly during the first 5 hr of scotophase. Overall, ca. 50% of the responding moths also landed on the chemical dispenser; ca. 50% of the moths that landed also deposited eggs. There were no significant differences in the behavioral responses of females mating only once and those that had mated two or more times. Virgin females and male moths were significantly less responsive to the groundcherry attractant than mated females. The flight tunnel bioassay described provides an excellent system for evaluating plant allelochemics associated with host-plant selection.This article reports the results of research only. Mention of a proprietary product does not constitute an endorsement or the recommendation for its use by USDA.     

Identification of a sex pheromone ofHeliothis subflexa (GN.) (Lepidoptera: Noctuidae) and field trapping studies using different blends of components

Eight compounds were isolated from the sex pheromone gland ofHeliothis subflexa (Gn.) and identified as hexadecanal, (Z)-9-hexadecenal, (Z)-11-hexadecenal, (Z)-7-hexadecen-1-ol acetate, (Z)-9-hexadecen-1-ol acetate, (Z)-11-hexadecen-1-ol acetate, (Z)-9-hexadecen-1-ol, and (Z)-11-hexadecen-1-ol. Although the whole blend was found to be an effective male attractant, the deletion of alcohols from the blend increased trap captures considerably. Further, although the binary mixture of (Z)-9-hexadecenal and (Z)-11-hexadecenal caught some maleH. subflexa, significant increases in captures were noted when the three acetate components were included in the blend.Mention of a commercial or proprietary product in this paper does not constitute an endorsement of that product by the USDA or the State of Florida.     

Identification of sex pheromone components ofSpodoptera sunia Guenée (Lepidoptera: Noctuidae)

Moths belonging to the speciesSpodoptera sunia have been recognized as a new pest of cotton in Central America. By means of electro-physiologic investigations, solid sample injection gas chromatography, and combined gas chromatography-mass spectrometry, (Z)-9-tetradecenyl acetate, (9Z,12E)-9,12-tetradecadienyl acetate, (Z)-9-tetradecen-1-ol, and (Z)-11-hexadecenyl acetate, in a ratio of 10053120, were identified in the pheromone gland of female insects. These substances should serve as a base for the development of a pheromone-monitoring system for this lepidopteran pest.Pheromones, 60. Pheromones 59: Bestmann, HJ., Attygalle, A.B., Brosche, T., Erler, J., Platz, H., Schwarz, J., Vostrowsky, O., Wu Cai-Hong, Kaissling, K.E. and Chen Te-Ming. 1987. Z.Naturforsch. 42c:631–636.     

Production of pheromone by hairpencil glands of males obtained from interspecific hybridization betweenHeliothis virescens andH. subflexa (Lepidoptera: Noctuidae)

Pheromone produced by the hairpencil glands of interspecific hybrid- and backcross-generation males from crosses betweenHeliothis virescens (F.) withH. subflexa (Gn.) was studied. Males of reciprocal F₁ hybrids, all of which had hairpencil glands morphologically similar to those ofH. virescens, produced neither the same pheromone blend nor amounts of pheromone that were produced by males ofH. virescens. Instead, these hybrid males produced pheromone that was quantitatively and qualitatively similar to that produced byH. subflexa. Hairpencil gland extracts from males obtained from backcrossing F₁ females of either cross to males ofH. subflexa were the same as those ofH. subflexa. However, extracts from backcross males of crosses between F₁ females andH. virescens were variable. Some extracts from these backcross males were like those ofH. virescens while others were either likeH. subflexa or were intermediate between those of the parent species. These results showed that the production of pheromone by the hairpencil glands of hybrid and backcross males is under the dominant regulation of autosomal genes of theH. subflexa genome.     

Sex pheromone of the cranberry girdler,Chrysoteuchia topiaria (Zeller) (Lepidoptera: Pyralidae)

Z-11-Hexadecen-1-al (Z11-16A1), free of theE isomer, was identified in extracts of femaleChrysoteuchia topiaria (Zeller) abdominal tips. In commercial grass seed fields, traps baited with synthetic Z11-16A1 were almost as attractive as female-baited traps. An alcohol, thought to be Z-11-hexadecen-1-ol on the basis of gas Chromatographic retention times, was also isolated from the extract.     

(Z,E)-3,5-Tetradecadien-1-ol acetate sex attractant for the carpenterworm moth,prionoxystus robiniae (peck) (Lepidoptera: Cossidae)

Electroantennogram analyses of female gland extract and of male antennal responses to synthetic standards suggested that (Z,E)-3,5-tetradecadien-1-ol acetate is a pheromone component for the carpenterworm moth,Prionoxystus robiniae (Peck). The four 3,5-geometrical isomers were synthesized and bioassayed in the laboratory and the field in 1972, 1973, and 1974. TheZ,E isomer was found to be active in the laboratory and a good attractant in the field. The synthesis of theZ,E isomer also produced considerable quantities of theE,E isomer, which is difficult to remove completely. TheE,E isomer does not inhibit the response of males to theZ,E isomer when it is present in amounts up to 20% of theZ,E isomer. The addition of a keeper, a volatility modifier, or an antioxidant prolonged the activity of the attractant for as much as 43 days. (Z,E)-3,5-Tetradecadien-1-ol acetate may be a natural pheromone, but it has not been chemically defined from female extract. There is EAG evidence that a second pheromonal component may be present. The attractant nevertheless provides a tool for population survey, behavioral studies, evaluation of economic impact, and possibly control.     

Sex pheromone of the armyworm,Pseudaletia unipuncta (Haworth) (Lepidoptera: Noctuidae)

(Z)-11-Hexadecen-1-ol acetate (Z11–16Ac) free of theE isomer (<1%), hexadecan-1-ol acetate (16 Ac), and a hexadecen-1-ol [the (Z)-11 isomer based on the retention time on a Carbowax capillary column] were identified in extracts of the sex pheromone glands of adult virgin female armyworms,Pseudaletia unipuncta. Also, gas Chromatographic retention times on polar and nonpolar columns indicated the possible presence of (Z)-9-hexadecen-1-ol acetate (Z9–16Ac). The ratioZ11–16Ac/16Ac/Z11–16OH/Z9–16Ac was 10.150.130.02. Infield testsZ11–16 Ac was attractive alone, and the addition ofZ9–16Ac,Zll–16 OH, or 16 Ac singly or in combination in ratios found in the gland did not increase trap capture.Mention of a proprietary product does not constitute an endorsement of this product by the USDA.     

Constituents of wing gland and abdominal hair pencil secretions of male African sugarcane borer,Eldana saccharina walker (Lepidoptera: Pyralidae)

In addition totrans-3,7-dimethyl-6-octen-4-olide (eldanolide), vanillin, and 4-hydroxybenzaldehyde, identified by French workers in the wing gland and abdominal hair pencil secretions of the male African sugarcane borer,Eldana saccharina, we have, in an earlier note, reported the presence of several other terpenoid, aromatic, and unbranched-chain compounds such as, (Z)-3,7-dimethylocta-2,6-dienoic acid, 6,10,14-trimethyl-2-pentadecanol, 4-hydroxy-3-methoxybenzyl alcohol, 1-octadecane thiol, 16-hexadecanolide, and 18-octadecanolide in these secretions. In the present paper experimental details and spectral evidence supporting the identification of these compounds, as well as the identification of (Z)-9-hexadecenal and cw-3,7-di-methyl-6-octen-4-olide (cis-eldanolide), are reported. Using electroantennography it was found that male and female antennae reacted approximately equally strongly to both secretions. This result was confirmed in analyses of the secretions using coupled gas chromatography-electroantennography and it was found that male as well as female antennae responded to eldanolide. Vanillin, substituted phenols related to vanillin, and some oxygenated monoterpenes elicited weak responses in male and female antennae. In some analyses 6,10,14-trimethyl-2-pentadecanol, present in the secretions of the insect, gave a strong antennal response. The results obtained in dynamic and static headspace determinations showed that several of the organic compounds present in the glandular secretions are released in detectable quantities and are present in widely varying quantitative ratios in the effluvia of individual calling male moths.     

Interactions between pheromone traps with different strength lures for the pine beauty moth,Panolis flammea (Lepidoptera: Noctuidae)

Catches of malePanolis flammea in traps baited with lures containing 25 g of sex attractant are enhanced when in the proximity of traps baited with 125-g lures. The degree of enhancement is increased as the intertrap distance is decreased, and when the low-dose trap is upwind of the high-dose one. The patterns of alteration in trap catch suggest that moths initially attracted by one lure may divert into other traps, which may be either upwind of the original trap (overshooting), or downwind (undershooting). Overshooting can result in up to fivefold increases in catch and may provide a useful method for estimating the attractant zone of particular lure/trap combinations.     

Identification of sex pheromone of browntail moth,Euproctis chrysorrhoea (L.) (Lepidoptera: Lymantriidae)

A unique sex attractant pheromone was isolated and identified from extracts of ovipositor tips from the female browntail moth (Lepidoptera: Lymantriidae). The pheromone compound, (Z,Z,Z,Z)-7,13,16,19-docosatetraen-1-ol isobutyrate, CH₃CH₂CH=CHCH₂CH=CHCH₂CH= CH(CH₂)₄CH=CH(CH₂)₆O₂CCH(CH₃)₂, was identified by a combination of gas chromatography, mass spectrometry, and microreactions and was confirmed by synthesis. Traps baited with 5–50 g of the synthetic pheromone, dispensed from rubber septa treated with an antioxidant and a UV stabilizer, gave male moth captures that were comparable to traps baited with three virgin females. Higher (250 g) and lower (0.04–2.5 g quantities of the synthetic pheromone on septa captured somewhat fewer males. Captures were the same for similar quantities of the natural and synthetic pheromone. Minor, inactive components in the tip extract were identified as a mixture of 7- and 8-pentacosanone.     

Identification of sex pheromones of two sibling species in dingy cutworm complex,Feltia jaculifera (GN.) (Lepidoptera: Noctuidae)

The sex pheromone components of the two sibling species of the dingy cutworm that occur on the prairies of western Canada were identified in abdomen-tip extracts from calling female moths. Three monounsaturated acetates, (Z)-7-dodecenyl acetate, (Z)-9-tetradecenyl acetate, and (Z)-11-hexadecenyl acetate, are common to both species in ratios of 100133 for species A and 0.30.5100 for species B. The most effective synthetic blends for the attraction of male moths in the field consisted of these three components in ratios of 1010 at 8.8g/lure for species A and 112000 at 500g/lure for species B. The addition of Z5-12Ac to either blend reduced the catches and the addition of Z7-12OH orZ11-16OH to the three-component blend reduced the catches of species B males. The species are morphologically indistinguishable, but the identity of the males attracted to the synthetic blends could be confirmed by their antennal responses to a test blend of the three components using a GC-EAD system. Both synthetic attractant blends are competitive with females and will be useful for studying the distribution, biology, and relative abundances of the two species.Contribution no. 3879005 of the Lethbridge Research Station.     

Multispecies trapping ofHelicoverpa (Heliothis) zea,Spodoptera frugiperda,Pseudaletia unipuncta,andAgrotis ipsilon (Lepidoptera: Noctuidae)

Multispecies sex pheromone trapping (trapping of more than one species in the same trap) for the bollworm,Helicoverpa (Heliothis) zea (Boddie); fall armyworm,Spodoptera frugiperda (J.E. Smith); armyworm,Pseudaletia unipuncta (Haworth); and the black cutworm,Agrotis ipsilon (Hufnagel) was evaluated. Baiting of individual traps with all possible combinations of the four species taken two at a time caused a reduction in the catches of at least one of any two species involved when compared to traps baited for only one species. These results demonstrated the species specificity of sex pheromones identified for these species. Although the effects were reduced in some cases, the interaction between species also was observed when adjacent traps were baited with the sex pheromone dispensers of the different species. These results indicate that the spacing between pheromone traps when more than one species are being trapped at the same site affects trap capture and should be evaluated further.This paper reports the results of research only. Mention of a commercial or proprietary product does not constitute an endorsement by the USDA.     

Female sex pheromone components ofHeliothis peltigera (Lepidoptera: Noctuidae)

Ten compounds were found in the sex pheromone glands ofHeliothis peltigera (Schiff) and identified as tetradecenal, (Z)-9-tetradecenal, (Z)-9-tetradecenol, (Z)-9-tetradecenyl acetate, hexadecanal, (Z)-7-hiexadecenal, (Z)-9-hexadecenal, (Z)-11-hexadecenal, (Z)-11-hexadecenol, and (Z)-11-hexadecenyl acetate. Behavioral tests in a wind tunnel and subsequent trapping studies conducted in the field indicated that (Z)-11-hexadecenal and (Z)-9-tetradecenal are the main pheromone components ofH. peltigera. Addition of (Z)-11-hexadecenol to the binary blend did not enhance the capture of males ofH. peltigera, but it decreased the number of males of the sympatricH. armigera. Rubber septa impregnated with a mixture of 2 mg (Z)-11-hexadecenal + 1 mg (Z)-9-tetradecenal + 0.6 mg (Z)-11-hexadecenol are recommended for monitoringH. peltigera. Contribution from the Agricultural Research Organization (ARO), No. 2454-E, 1988 series.     

Identification of female sex pheromone components of rice looper,Plusia festucae (L.), (Lepidoptera: Noctuidae)

The rice looper,Plusia festucae, is a defoliator of the rice plant. Chromatographic behavior, chemical reactions, and GC-MS analyses of the female sex pheromone revealed that the main component was (Z)-5-dodecenyl acetate (Z5–12: OAc, component I). The GC-MS analysis also indicated that the pheromone gland extract included another three monounsaturated components, (Z)-5-dodecen-l-ol (Z5–12: OH, component II), (Z)-7-tetradecenyl acetate (Z7–14: OAc, component III), and (Z)-7-tetradecen-l-ol (Z7–14: OH, component IV) in the following ratio: I:II:III:IV=100:6:15:1. In a paddy field, the mixture of synthetic I, II, and III in a ratio of 100:6:15 showed stronger attractancy than the virgin female, while the role of IV was unknown.     

Electroantennographic responses differentiate sibling species of dingy cutworm complex,Feltia jaculifera (GN.) (Lepidoptera: Noctuidae)

The dingy cutworm is one of the more common and widely distributed of North American noctuids. Determination of the antennal responses of field-collected male moths to a standard test blend of pheromone components shows that two pheromonal phenotypes of the dingy cutworm occur throughout the prairie region of western Canada and at least two others occur in eastern Canada. The pheromone types are morphologically indistinguishable and, so far as is known, have similar life histories and biology. The two prairie types are broadly sympatric with partially overlapping seasonal flight periods. Although hybrids can be easily produced in the laboratory, there is no evidence of hybridization in the field. The pheromone system of the dingy cutworm is apparently rather plastic, resulting in a mosaic of pheromone types (sibling species) that appear to be reproductively isolated but have not differentiated morphologically.Contribution no. 3878948 of the Lethbridge Research Station.     

Sex attractant for three species of the genusOncocnemis: O. chandleri (Grt.),O. cibalis (Grt.), andO. mackiei (B. & Benj.) (Lepidoptera: Noctuidae)

Oncocnemis chandleri, O. cibalis, andO. mackiei were attracted to chemically baited traps in the field. In all three cases, (5E,7Z)-dodecadienyl acetate was a key component for attraction. Attraction ofO. chandleri to traps baited with the (5E,7Z)-dodecadienyl acetate was inhibited by addition of (Z)-7-dodecenyl acetate.O. cibalis required both (5E,7Z)-dodecadienyl acetate and (Z)-7-dodecenyl acetate for attraction. Electroantennogram responses for the three species are also reported.