Intrapopulational changes in sex pheromone composition during scotophase in oriental tobacco budworm,Helicoverpa assulta (Guenée) (Lepidoptera: Noctuidae)

Solvent extracts of individual pheromone glands were prepared from femaleHelicoverpa assulta (Guenée) at 2-hr intervals throughout the scotophase. The amounts of female sex pheromone components, (Z)-9-hexadecenal, (Z)-11-hexadecenal, (Z)-9-hexadecenyl acetate, and (Z)-11-hexadecenyl acetate, in the extracts were determined by gas chromatographic analysis. Although females called from early scotophase (2 hr) until late scotophase (6 hr) the quantity of extracted pheromone remained high at 8 hr, the end of the scotophase. More than 70% of the pheromone gland extracts contained sex pheromone components regardless of whether the donor females had been called or resting. Pheromone components were absent from gland extracts prepared at the onset of the scotophase. The quantity of (Z)-9-hexadecenal and (Z)-11-hexadecenal increased rapidly to reach a maximum of approximately 260 and 30 ng/female, respectively, that was maintained for up to 8 hr, the duration of the scotophase. The quantity of (Z)-9-hexadecenyl acetate and (Z)-11-hexadecenyl acetate increased continuously during the scotophase to peak at 600 and 30 ng/female, respectively, 8 hr into the scotophase. At the end of scotophase the quantity of all pheromone components decreased significantly.     

Identification of Sex Pheromone of Adzuki Bean Borer,Ostrinia scapulalis

By means of gas chromatography with electroantennographic detection (GC-EAD), gas chromatography–mass spectrometry (GC-MS), and a series of bioassays, (Z)-11-tetradecenyl acetate (Z11–14:OAc) and (E)-11-tetradecenyl acetate (E11–14:OAc) at a ratio of 100:3 were identified as the female sex pheromone of the adzuki bean borer,Ostrinia scapulalis. The average amounts ofZ11–14: OAc andE11–14:OAc in a single sex pheromone gland were 6.6 ± 2.4 ng and 0.2 ± 0.1 ng, respectively. In a wind-tunnel bioassay, the binary blend ofZ11- andE11–14:OAc elicited almost the same male behavioral responses as did virgin females and sex pheromone gland extract. In field trapping experiments, rubber septa impregnated with the binary blend (50 g/septum) attracted more males than virgin females. The sex pheromone ofO. scapulalis thus turned out to be similar to that of theZ-type European corn borer,O. nubilalis, in both components and their ratio.     

Diel periodicity and influence of age and mating on sex pheromone titer in gypsy moth,Lymantria dispar (L.)

The diel periodicity of sex pheromone titer from pheromone glands of femaleLymantria dispar is described. On the day of emergence (day 0), pheromone titer was generally low; means ranged from 1 to 4 ngcis- 7,8-epoxy-2-methyloctadecane during photophase and gradually increased to 8.4 ng over the course of scotophase. For day-1, -2, and -3 females, the diel fluctuations of titer were more pronounced. Lowest titers (5–9 ng) occurred 0–4 hr after lights-on, and peak titers (19–32 ng) were found 0–4 hr before lights-off. Comparison of the average daily titer among the different age groups (data pooled over six time points at 4-hr intervals) indicated that significantly less pheromone was extracted from glands of day-0 (4.5 ng) than day-1 (12.4 ng), day-2 (15.4 ng), or day-3 females (13.5 ng). No significant differences were found among the three older ages. Femalesin copula exhibited a rapid reduction in titer within the first 0.5 hr of mating initiation (7.6 ng vs. 19.5 ng from virgin females of similar age). After the second 0.5 hr, the reduction in titer was not nearly as marked, falling only to 4.5 ng. Twenty-four hours after mating, titer fell below the limits of detection (0.5 ng). All extracts from pheromone glands of virgin or mated females contained < 1.0 ng of the putative pheromone precursor, 2-methyl-cis-7-octadecene.     

Sex pheromone of cranberry fruitworm,Acrobasis vaccinii riley (Lepidoptera: Pyralidae)

The following compounds and (approximate ratios) were identified in sex pheromone gland extracts of femaleAcrobasis vaccinii Riley by comparison of gas chromatography-mass spectrometric traces with those of synthetic standards: (E,Z)-, (Z,E)-, (Z,Z), and (E,E)-8, 10-pentadecadien-l-ol acetates (100:1:2:12), a dodecen-l-ol acetate (8), (Z)-8-, (Z)-9-, and (E)-9-pentadecen-l-ol acetates (3:23:4), two heptadecen-l-ol acetates (4:4), tetradecyl, pentadecyl, hexadecyl, and heptadecyl acetates (3:15:10:8), dodecan-l-ol (6), tetradecan-l-ol (5), and hexadecan-l-ol (23). The amount of (E,Z)-8, 10-pentadecadien-l-ol acetate (E8,Z10–15:Ac) in the extract was about 0.5 ng/female. Electroantennographic analysis of gas chromatographic fractions of female sex pheromone gland extract showed that the fraction containingE8,Z10–15:Ac elicited the greatest response. Alone,E8,Z10–15:Ac failed to elicit upwind flight of males in flight-tunnel tests, and traps baited with it did not catch males in field experiments. WhenE8,Z10–15:Ac was combined with (E)-9-pentadecen-l-ol acetate (100:4), male upwind flight response in flight-tunnel tests was equivalent to those obtained with extract of female sex pheromone glands (synthetic, 62%; natural, 51%), but the percent of males flying upwind that contacted the source was lower (synthetic, 47%; natural, 88%). The lower percent of source contact elicited by the synthetic pheromone could be a result of the difference in isomer ratios of 8,10–15:Ac in the natural and synthetic pheromone or could indicate that the synthetic pheromone is incomplete. Traps baited with the 100:4 combination caught large numbers of males in field experiments.     

Composition,quantification, and periodicity of sex pheromone gland volatiles from individualHeliothis virescens females

Sex pheromone gland volatiles from individualHeliothis virescens (F.) females were collected and analyzed on an SP-2330 capillary gas-liquid chromatography column for identification and quantification of the compounds emitted. Only four of the seven compounds previously reported as pheromone components appeared consistently in the volatile collections: 14:Ald, Z9-14:Ald, 16:Ald, and Z11-16:Ald. The female glands did not emit the same amounts of these compounds throughout a 24-hr period; they emitted maximum quantities between 6 and 11 hr after the onset of scotophase with the remainder of the photoperiod having minimal emission rates. Although the absolute quantities fluctuated, the percent compositions of the compounds remained about the same throughout the 24-hr period.     

Eversible Pheromone Gland in a Melolonthine Beetle, Holotrichia parallela

The morphology of an eversible pheromone gland of a melolonthine beetle, Holotrichia parallela (Coleoptera: Scarabaeidae: Melolonthinae), was characterized. Through careful dissection of the gland and GC-MS analysis of tissue extracts, we determined that the pheromone is produced in the posterior part of a ball-shaped sac exposed during female calling. Light microscope observation of the posterior part of the gland revealed a layer of cuticular epithelium composed of columnar cells, which was assigned as the tissue involved in pheromone production. Other morphological features, such as a soft cuticular layer adjacent to the epithelium and groups of retractor muscles attached to the gland, were characterized according to their functions. Paired accessory glands, which in some other melolonthine species house symbiotic bacteria that produce a sex attractant, were found not to be involved in pheromone production in H. parallela.     

Sex Pheromone Components of Pitch Pine Looper, Lambdina pellucidaria

Two methylated hydrocarbons, 7-methylheptadecane (7) and 7,11-dimethylheptadecane (7,11), are sex pheromone components of female pitch pine looper (PPL), Lambdina pellucidaria. Compounds extracted from the pheromone glands of female moths were identified by coupled gas chromatographic–electroantennographic detection (GC-EAD) and coupled GC–mass spectrometry (GC-MS) in selected ion monitoring mode. In field-trapping experiments, 7 and 7,11 in combination, but not singly, attracted numerous male moths. 5,11-Dimethylheptadecane (5,11) was detected by GC-EAD in female PPL pheromone gland extract, but did not significantly increase attraction of PPL males to 7 plus 7,11. Although 7 was > 10 times more abundant than 7,11 in pheromone gland extracts, traps baited with synthetic 7 plus 7,11 at a blend ratio of 1:1, rather than 1:0.1 or 1:0.01, captured the most PPL males. The chemical communication of PPL and spring hemlock looper (SHL), Lambdina athasaria, is strikingly similar. Both species employ 7 plus 7,11 as sex pheromone. Restriction of SHL to forests with eastern hemlock or balsam fir and PPL to forests with pitch or other hard pines contributes to their reproductive isolation. PPL and SHL may also use different optical isomers of enantiomeric 7 and stereoisomeric 7,11 to maintain specificity of their chemical communication.     

Unusual periodicity of sex pheromone production in the large black chaferHolotrichia parallela

(R)-(–)-Linalool was identified as a minor component sex pheromone of the scarab beetleHolotrichia parallela (Coleoptera: Scarabaeidae). Field evaluations revealed that, although not attractive per se, (R)-(–)-linalool enhances the attractiveness of the major sex pheromone,L-isoleucine methyl ester (LIME). Analyses of the pheromone titers in the glands of field-collected females demonstrated the occurrence of peak levels of 48-hr (circabidian) periodicity. The levels of LIME in the glands of 45-day-old virgin females increased over three times from the scototo the photophase of a calling day, but the amounts of (R)-(–)-linalool did not significantly change. Virgin females had in average two times more LIME and 3.6 times more (R)-(–)-linalool than the average amount found in the field-captured beetles throughout the season.     

Rosefuran: The Sex Pheromone of an Acarid Mite, Caloglyphus Sp.

Rosefuran was identified as a female sex pheromone from an unnamed species of acarid mite, Caloglyphus sp., whose phoretic hypopi had been collected from the elongated yellowish chafer, Heptophylla picea. Behavior of sexually excited males was demonstrated by exposing them to doses of 1–100 ng of synthetic rosefuran. The pheromone was present in females and also in males and was detected in trace amounts in nymphal stages. Pheromone concentrations were estimated to be 87 ± 14.2 ng per female and 10.4 ± 2.5 ng per male. The quantitative difference between sexes may allow males to discriminate females for purposes of mating.     

Variability in pheromone composition and periodicity of pheromone titer in potato tuberworm moth,Phthorimaea operculella (Lepidoptera: Gelechiidae)

The ratios and quantities of the pheromone components, (E,Z)-4,7-tridecadien-1-yl acetate (diene) and (E,Z,Z)-4,7.10-tridecatrien-1-yl acetate (triene), in the glands of individual female potato tuberworm moths (Phthorimaea operculella) originating from the United States (California) and Japan (Nagoya) were analyzed by gas chromatography. Quantities of glandextracted pheromone components of Nagoya females fluctuated in a periodic fashion during the photoperiod. Maximal titers coincided with the onset of scotophase (and calling), then gradually declined to minimal levels soon after lights-on. The average daily pheromone quantities decreased significantly as females aged. Both populations exhibited considerable variation in the ratio of the two components. The proportions of triene in the blend ranged from 27% to 88% (triene –X = 56 ± 13% SD; CV = 23%) for California females and from 16% to 71% (42 ± 13%; CV = 31%) for Nagoya females. Nagoya females also stored significantly higher amounts of pheromone in their glands (8.6 ± 3.9 ng) than did California females (2.7 ± 1.4). The differences between the populations, while substantial, would probably not be sufficient to impart a barrier to panmixis, given the wide range of component ratios favored by the males.     

Calling behavior and pheromone titer in the smaller tea tortrix moth,Adoxophyes sp. (Lepidoptera: Tortricidae)

The calling behavior and pheromone titer in the female smaller tea tortrix moth,Adoxophyes sp., were investigated under a 1410-hr light-dark photoperiod. Quantitative gas chromatographic analysis of ovipositor extract for (Z)-11-tetradecenyl acetate (Z11–14Ac) and (Z)-9-tetradecenyl acetate (Z9–14Ac), the major pheromone components of this species, obtained on the third day postemergence, indicated that extractable amounts of sex pheromone were present throughout the period of observation. Maximal pheromone titer and calling activity was reached at 8 and 10 hr after onset of scotophase, respectively. The ratio ofZ11–14Ac toZ9–14Ac through the 24-hr period varied significantly. The significance of the sex pheromone component ratio variation on the attraction of males was tested in a field experiment. The ratio of males trapped by the most attractive blend versus the least attractive one was 2.16.     

Sex pheromone of purplestriped shootworm,Zeiraphera unfortunana powell

The analyses of virgin female sex pheromone gland extracts and gland volatiles by GC, GC-EAD and GC-MS, followed by field trapping experiments, have identified (E)-9-dodecenyl acetate (E9–12Ac) as the primary sex pheromone component of the purplestriped shootworm,Zeiraphera unfortunana. Dosages of 1.0–10.0 g ofE9–12Ac impregnated in rubber septa provide an effective trap bait and can be used for monitoring purposes.Lepidoptera: Tortricidae.     

Foveal glands,source of sex pheromone production in the ixodid tickDermacentor andersoni stiles

The foveal glands of the Rocky Mountain wood tick,Dermacentor andersoni Stiles, are the sex pheromone glands from which the sex pheromone is released via the foveae dorsales. The sex pheromone, 2,6-dichlorophenol, was recovered from extracts of these glands by GLC. Other evidence of the role of these glands in sex pheromone production is described. A³⁶Cl-labelled volatile compound (or compounds) was (were) collected from partially engorged femaleD. andersoni fed in³⁶Cl-labelled hosts, but no labelled compounds were collected when the foveae dorsales were blocked. X-ray analysis revealed unusual concentrations of chlorine in the foveal glands compared to other tissues. Autoradiography also revealed significant accumulations of radiochlorine in the vicinity of these glands.Presumably, the foveal glands of the American dog tick,Dermacentor variabilis (Say), are the sex pheromone glands of that species also, since a³⁶Cl-labelled volatile was collected from female ticks fed on a³⁶Cl-labelled host. However, attempts to recover 2,6-dichlorophenol from gland extracts or volatile emissions fromD. variabilis were unsuccessful.Supported by grants AI 10,986 and AI 10,987 from the National Institute of Allergy and Infectious Diseases, U.S. Public Health Service, U.S. Department of Health, Education and Welfare, Bethesda, Maryland, 20014.     

(E)-11,13-tetradecadienal: Major sex pheromone component of the eastern blackheaded budworm,Acleris variana (Fern.) (Lepidoptera: Tortricidae)

(E)-11,13-Tetradecadienal (E11,13–14:Ald) is the major sex pheromone component of the eastern blackheaded budworm (EBB),Acleris variana (Fern.). The compound was identified in female pheromone gland extracts by coupled gas chromatographic-electroantennographic detection (GC-EAD), coupled GC-mass spectrometry in selected ion monitoring mode, and retention index calculations of candidate pheromone components.E11,13–14:Ald alone as trap bait was very attractive to male EBB. Addition of the corresponding diene alcohol or acetate or both did not enhance attraction. (Z)-11,13-Tetradecadienal in binary combination with (E)-11,13–14:Ald neither enhanced nor reduced trap catches. Increasing the amounts of pheromone from 0.01 to 10 µg increased trap catches, but increase of pheromone quantity above 100 µg proportionately reduced attraction. Stabilization of slowly polymerizingE11,13–14:Ald and development of a sustained, adequate release rate is required for pheromone-based monitoring of EBB populations.     

Sex pheromone components of the buck moth Hemileuca maia

The sex attractant pheromone blend of Hemileuca maia (Lepidoptera: Saturniidae) from the vicinity of Baton Rouge, Louisiana, has been identified. The major component of the blend is (E10,Z12)-hexadeca-10,12-dienal (E10,Z12–16:Ald), in combination with the minor components (E10,Z12)-hexadeca-10,12-dien-1-ol (E10,Z12–16:OH), and (E10,Z12)-hexadeca-10,12-dien-1-yl acetate (E10,Z12–16:Ac). Ratios of the compounds in extracts of female pheromone glands varied around a mean of 100:7.4:6.3. None of the three components were attractive to male moths when tested as single components. Several other compounds were tentatively identified from female pheromone gland extracts, including E10,E12–16:Ald, E10,E12–16:OH, and E10,E12–16:Ac, but addition of these components, either alone or in combination, at biologically relevant rates, did not significantly increase the attractiveness of lures. The saturated analogs, hexadecanal, hexadecanol, and hexadecyl acetate, also were identified in gland extracts, but had no apparent effect as pheromone components.     

Female Sex Pheromone Polymorphism in Adzuki Bean Borer, Ostrinia scapulalis, Is Similar to That in European Corn Borer, O. nubilalis

Individual analysis of the female sex pheromone of the adzuki bean borer, Ostrinia scapulalis, has shown that the sex pheromone of this species comprised (E)-11-tetradecenyl acetate (E11–14:OAc) and (Z)-11-tetradecenyl acetate (Z11–14:OAc) at variable blend ratios. The pheromone blend could be tentatively categorized into three types with respect to the proportion of E11–14:OAc: E type (94–100%, median 99.2%), Z type (0–16%, median 3.0%), and intermediate type (I type, 48–85%, median 63.7%). In addition to the identity of components, the blend ratios in the three types were similar to those of the E strain, Z strain, and hybrid of the European corn borer, O. nubilalis, respectively. This finding suggests that two closely related but morphologically distinct species, O. scapulalis and O. nubilalis, share almost the same sex pheromone communication systems. The significance of this similarity in the two sibling species is discussed.     

Identification of sex pheromone of bristly cutworm,Lacinipolia renigera (Stephens)

The sex pheromone of the bristly cutworm moth,Lacinipolia renigera was identified as a blend of (Z)-9-tetradecenyl acetate (itZ9–14): Ac and (Z, E)-9,12-tetradecadienyl acetate (ZE-9,12–14: Ac). Extracts of female glands were analyzed by capillary gas chromatography on three columns of different polarities. In each analysis, peaks with retention times identical to Z9–14:Ac andZE–9, 12–14: Ac were observed. GC-MS analysis of gland extracts supported the identification of these two compounds. Volatiles emitted from female sex pheromone glands during 10-min collection periods contained 7.8 ±2.01 ng ofZ9- 14: Ac. On average the blend contained 3.8 ± 1.43%ZE-9,12–14: Ac. Blends ranging from 1% to 10%ZE- 9,12–14: Ac in Z9-14: Ac (1 mg) were effective in capturing males in the field. The number of males captured in traps baited with a 3 % blend ofZE- 9,12-14: Ac in Z9-14: Ac was not significantly different than the number caught in traps containing two virgin females.     

On-line Thermal Desorption–Gas Chromatography of Intact Insects for Pheromone Analysis

By using a thermodesorption system (TDS) together with a programmable temperature vaporizer (PTV) injector, we confirmed the composition of the sex pheromone of Adoxophyes orana (Lepidoptera: Tortricidae) and Campylomma verbasci (Heteroptera: Miridae) from a single insect per analysis. Intact females and males or pheromone glands were placed in the oven part of the TDS, which was subsequently heated. The compounds released were transferred to the PTV, which was cooled to –150°C. Injection was on a dual-column GC by heating the PTV rapidly to 250°C. The major sex pheromone compounds of A. orana were found only in the pheromone gland of females. Male and female C. verbasci showed fingerprint-identical chromatograms, except for the two sex pheromone compounds, which were present only in females. No distinct differences were found in compounds released from female and male Lygocoris pabulinus (Heteroptera: Miridae). The advantages of this rapid method are the high sensitivity and the low degree of degradation and contamination. This technique was effective in analyzing small insects by gas chromatography–mass spectrometry (GC-MS) without prior manipulation, such as solvent extraction or distillation.     

Production and release of (Z,E)-9,12-tetradecadienal by sex pheromone glands of females ofPlodia interpunctella (lepidoptera: pyralidae)

Extracts of sex pheromone glands obtained from females ofPloida interpunctella contained detectable amounts of (Z,E,)-9,12-tetradecadien-1-ol acetate (Z9,E12–14:Ac) and (Z,E.)-9,12-tetradecadien-1-ol (Z9,E12–14:OH) 4 hr prior to the first scotophase after adult emergence. The amount of pheromone increased during the first 4 hr of the scotophase and then declined to low levels during the subsequent photophase. Decapitation of females immediately after emergence, prior to expansion of the wings, inhibited production of pheromone during the subsequent 48 hr. Injection of extracts of the heads of 1-day-old females ofP. interpunctella of partially purified extracts of the cephalic ganglia of females of the corn earworm moth into decapitated females stimulated production of bothZ9,E12–14:Ac andZ9,E12–14:OH as well as production of (Z,E)-9,12-tetradecadienal (Z9,E12–14:Al). This aldehyde was subsequently identified from extracts of pheromone glands obtained from naturally calling females as well as from volatiles emitted by calling females. Studies on the terminal steps in biosynthesis of the pheromone showed thatZ9,E12–14:OH was produced from the corresponding acetate and thatZ9,E12–14:Al was produced from the alcohol via the action of an oxidase(s).     

Identification of sex pheromone component of spruce budmothZeiraphera canadensis

The analyses of virgin female sex pheromone gland extracts by gas chromatography (GC), GC-electroantennographic detection (GC-EAD) and GC-mass spectrometry (GC-MS) followed by field-trapping experiments, have identified (E)-9-tetradecenyl acetate (E9–14:Ac) as the primary sex pheromone component of the spruce budmoth,Zeiraphera canadensis. Dosages of 1.0–100.0 g ofE9–14:Ac impregnated in rubber septa provide effective trap baits.Lepidoptera: Tortricidae: Eucosminae.