Le Van Vang

Synthesis and characterization of hexadecadienyl compounds with a conjugated diene system, sex pheromone of the persimmon fruit moth and related compounds.

Hexadecadien-1-ol and the derivatives (acetate and aldehyde) with a conjugated diene system have recently been identified from a pheromone gland extract of the persimmon fruit moth (Stathmopoda masinissa), a pest insect of persimmon fruits distributed in East Asia. The alcohol and acetate showed their base peaks at m/z 79 in a GC-MS analysis by electron impact ionization, but the aldehyde produced a unique base peak at m/z 84, suggesting a 4,6-diene structure. To confirm this inference, four geometrical isomers of each 4,6-hexadecadienyl compound were synthesized by two different routes in which one of two double bonds was furnished in a highly stereoselective manner. Separation of the two isomers synthesized together by each route was facilely accomplished by preparative HPLC. Their mass spectra coincided well with those of natural components, indicating that they were available for use as authentic standards for determining the configuration of the natural pheromone. Furthermore, other hexadecadienyl compounds, including the conjugated diene system between the 3- and 10-positions, were synthesized to accumulate the spectral data of pheromone candidates. 5,7-Hexadecadienal interestingly showed the base peak at m/z 80; meanwhile, the base peaks of its alcohol and acetate were detected at m/z 79 like the corresponding 4,6-dienes. The base peaks of all 6,8-, 7,9-, and 8,10-dienes universally appeared at m/z 67 like 9,11-, 10,12-, and 13,15-dienes, the spectra of which have already been published. Although 3,5-hexadecadienal was not prepared, base peaks at m/z 67 and 79 were recorded for the alcohol and acetate, respectively.

Sex pheromone of the persimmon fruit moth, Stathmopoda masinissa: Identification and laboratory bioassay of (4E, 6Z)-4,6-hexadecadien-1-ol derivatives

Three electroantennogram (EAG)-active components were detected by gas chromatography coupled to an electroantennographic detector (GC–EAD) analysis of a hexane extract of the pheromone glands of the persimmon fruit moth, Stathmopoda masinissa. These compounds were identified as (4E,6Z)-4,6-hexadecadienal (E4,Z6-16:Ald) and the corresponding acetate (E4,Z6-16: OAc) and alcohol (E4,Z6-16:OH) by mass spectral, GC retention time (RT), and microchemical test data. The characteristic base peak of the aldehyde at m/z 84 provided a crucial piece of information suggesting the possibility of a 4,6-diene structure. The (4E,6Z)-isomer elicited the strongest EAG responses among the four geometrical isomers of each synthetic 4,6-hexadecadienyl compound. In a laboratory bioassay, only E4,Z6-16:OAc elicited male moth behavioral activity significantly different from the control; the activity of the acetate was not affected by addition of the aldehyde and alcohol. A preliminary field trial confirmed that E4,Z6-16:OAc as a single component attracted male moths. The possible roles of E4,Z6-16:Ald and E4,Z6-16:OH as components of lures for field use remain to be determined.

Identification of the sex pheromone secreted by Synanthedon tenuis (Lepidoptera: Sesiidae)

The Japanese persimmon treeborer, Synanthedon tenuis (Butler) (Lepidoptera: Sesiidae), is a harmful pest of persimmon trees (Diospyros spp.). Because males of this species are known to be attracted by (3Z,13Z)-3,13-octadecadienyl acetate (Z3,Z13-18:OAc), a mating disruptant composed of a 1:1 mixture of Z3,Z13-18:OAc and the (3E,13Z)-isomer, the original target of which is an allied pest, S. hector (Butler), has been diverted to control S. tenuis. However, the sex pheromone secreted by S. tenuis females has not been characterized. Analyses of pheromone gland extracts using gas chromatography (GC) equipped with an electroantennographic detector (GC-EAD) and GC combined with mass spectrometry (GC–MS) detected only Z3,Z13-18:OAc, and no other known sesiid pheromone components were found. In a persimmon orchard, S. tenuis males were selectively attracted by a lure baited with Z3,Z13-18:OAc among four geometrical isomers of 3,13-octadecadienyl acetate, indicating that males strictly discriminated among the configurations of the two double bonds. Lures baited with single Z3,Z13-18:OAc attracted only S. tenuis. Further field experiments revealed that the attractiveness of Z3,Z13-18:OAc is significantly inhibited by the addition of the (3E,13Z) isomer or the parent alcohol.

Sex Pheromones of Five Olethreutine Species (Lepidoptera: Tortricidae) Associated with the Seedlings and Fruits of Mangrove Plants in the Ryukyu Islands, Japan: Identification and Field Evaluation

The sex pheromones of three Cryptophlebia, one Centroxena, and one Eucosma species (Lepidoptera: Olethreutinae) inhabiting mangroves in the Ryukyu Islands, Japan, were studied with coupled gas chromatography-electroantennographic detection, and GC-mass spectrometry (GC-MS). The larvae of each Cryptophlebia species are specifically associated with viviparous seedlings from one of three mangrove Rhizophoraceae plants. Whereas three EAG-active alcohol components, (Z)-8-dodecen-1-ol, (E)-8-dodecen-1-ol, and dodecan-1-ol, in a ratio of 100:12:4, were identified from the pheromone gland extract of female of C. horii (host: Bruguiera gymnorrhiza), two other sibling species produced the corresponding acetates, i.e., (Z)-8-dodecenyl acetate, (E)-8-dodecenyl acetate, and dodecyl acetate, in a 100:2:3 ratio from Cryptophlebia palustris (host: Rhizophora stylosa in Iriomote-jima Island) and in a 100:7:13 ratio from C. amamiana (host: Kandelia candel in Amami-oshima Island). The double bond positions of the monounsaturated components were confirmed by GC-MS analyses of their adducts with dimethyl disulfide. On the other hand, the larvae of Centroxena sp. feed on fruits of Sonneratia alba, another mangrove plant in the Sonneratiaceae, and the extract of the female pheromone glands contained (8E,10E)-dodecadienyl acetate and dodecyl acetate in a ratio of 100:5. The double bond position of the diunsaturated compound was confirmed by GC-MS analysis of its adduct with 4-methyl-1,2,4-triazoline-3,5-dione. (E)-9-Dodecenyl acetate was exclusively identified in the pheromone gland extract of Eucosma coniogramma females reared from seedlings of B. gymnorrhiza. Although the roles of minor components have not been revealed by field tests, synthetic lures baited with the main pheromone component of each species successfully attracted the target males, confirming that the sex pheromone is one of the most important factors for their reproductive isolation.

SEX ATTRACTANTS FOR MOTHS OF VIETNAM: FIELD ATTRACTION BY SYNTHETIC LURES BAITED WITH KNOWN LEPIDOPTERAN PHEROMONES

Screening tests of synthetic lepidopteran sex pheromones were carried out at orchards in the Mekong Delta over an approximately two-year period starting from December 1998. Monoenyl acetates with a C10–C14 chain attracted six species distributed mainly in Southeast Asia: Adoxophyes privatana, Archips atrolucens, and Meridemis furtiva in the Tortricidae family, and Argyrogramma signata, Spodoptera pectinicornis, and Zonoplusia ochreata in the Noctuidae family. These were in addition to three other noctuid species that had been attracted during previous field examinations within a temperate zone. Furthermore, male moths of three species belonging to the Cosmopterigidae, Gelechiidae, or Batrachedridae family were also caught by traps baited with acetates. Trienes with a C18–C21 chain and their monoepoxides, which are stereotypes of pheromones secreted by females in the Geometridae family, failed to attract any geometrid male, but attracted three Noctuidae species and four Arctiidae species.

Reexamination of the Female Sex Pheromone of the Sweet Potato Vine Borer Moth: Identification and Field Evaluation of a Tricosatriene

The sweet potato vine borer moth, Omphisa anastomosalis (Pyraloidea: Crambidae), is a serious pest in tropical and subtropical Asia-Pacific regions. In previous work using a population from Okinawa, Japan, (10E,14E)-10,14-hexadecadienal (E10,E14-16:Ald) was identified as the major pheromone component, with hexadecanal, (E)-10-hexadecenal, and (E)-14-hexadecenal as minor components. However, traps baited with the synthetic compounds were less effective at attracting males in the field than those baited with virgin females. While Pyraloidea females usually produce only Type I pheromone components (unsaturated fatty alcohols and their derivatives), the pheromones of some Pyraloidea species have been shown to involve a combination of both Type I and Type II components (unsaturated hydrocarbons and their epoxides). We examined an extract of the pheromone glands of female O. anastomosalis from Vietnam by gas chromatography coupled to mass spectrometry and detected (3Z,6Z,9Z)-3,6,9-tricosatriene (Z3,Z6,Z9-23:H) in addition to the compounds identified previously. All four isomers of 10,14–16:Ald were synthesized. A mixture of synthetic E10,E14-16:Ald and Z3,Z6,Z9-23:H in a ratio of 1:0.2–1:2 was attractive to male moths in Vietnam, indicating the strong synergistic effect of the Type II compound. Addition of the other minor pheromone components to the binary blend did not increase the number of male moths captured. Combinations of Z3,Z6,Z9-23:H with the other three geometrical isomers of E10,E14-16:Ald attracted no males, further substantiating the 10E,14E configuration of the natural diene component. E10,E14-16:Ald mixed with other polyunsaturated hydrocarbons showed that mixtures that included a C21 triene, a C22 triene, or a C23 pentaene attracted as many males as did the mixture with Z3,Z6,Z9-23:H. The identification of a highly attractive sex pheromone will help in developing efficient strategies for monitoring and control of O. anastomosalis populations in sweet potato fields.

Identification of Conjugated Pentadecadienals as Sex Pheromone Components of the Sphingid Moth, Dolbina tancrei

Homologs of bombykal, (10E,12Z)-10,12-hexadecadienal, have been reported to be sex pheromones or sexual attractants of several species of sphingid moths. In this study, we identified novel bombykal analogs as sex pheromone components from a Japanese sphingid moth, Dolbina tancrei. Staudinger (Sphingidae: Lepidoptera). Sex pheromone gland extracts from calling female moths were subjected to gas chromatography/electroantennograhic detection (GC/EAD), gas chromatography/mass spectrometry (GC/MS), and gas chromatography (GC) analyses. GC/EAD analyses showed two active components in the crude pheromone extracts. GC/MS analysis determined these two components to be pentadecadienals. GC/MS of their MTAD derivatives showed conjugated double bonds at the 9- and 11-positions, indicating 9,11-pentadecadienals. The isomeric configurations of these candidates were determined by comparison of their Kováts retention indices with those of synthetic compounds. Field bioassays with the four isomers of 9,11-pentadecadienal and their mixtures confirmed that the two sex pheromone components of D. tancrei are (9E,11Z)-9,11-pentadecadienal and (9Z,11Z)-9,11-pentadecadienal, with the highest male catches observed for a 90:10 blend. This is the first report of 9,11-pentadecadienals as sex pheromone components in lepidopteran species.

Sex Pheromones of Three Citrus Leafrollers, Archips atrolucens , Adoxophyes privatana, and Homona sp., Inhabiting the Mekong Delta of Vietnam

Archips atrolucens, Adoxophyes privatana, and Homona sp. are serious defoliators of citrus trees in the Mekong Delta of Vietnam. In order to establish a sustainable pest-management program for the three species, their female-produced sex pheromones were investigated by GC-EAD and GC-MS analyses, and the following multi-component pheromones were identified: (Z)-11-tetradecenyl acetate (Z11-14:OAc), (E)-11-tetradecenyl acetate (E11-14:OAc), and tetradecyl acetate (14:OAc) in a ratio of 64:32:4 for A. atrolucens; Z11-14:OAc and (Z)-9-tetradecenyl acetate (Z9-14:OAc) in a ratio of 92:8 for A. privatana; and Z11-14:OAc and (Z)-9-dodecenyl acetate (Z9-12:OAc) in a ratio of 96:4 for Homona sp. Each lure baited with synthetic components as a mimic of the natural pheromone attracted males of the target species specifically, indicating that each monounsaturated minor component plays a significant role for mating communication and reproductive isolation of the three species inhabiting the same citrus orchards. In an extract of the pheromone glands of A. atrolucens females, the content of 14:OAc was very low, but a synergistic effect was observed clearly when the saturated compound was mixed at the same level as the E11-14:OAc. The synthetic lures will provide useful tools for monitoring flights of adults of the three species.

Unsaturated Cuticular Hydrocarbon Components of the Sex Pheromone of Eggplant Fruit Borer, Leucinodes orbonalis Guenée (Lepidoptera: Crambidae)

Leucinodes orbonalis is one of the most damaging insect pests affecting eggplant in the Mekong Delta of Vietnam. While (E)-11-hexadecenyl acetate (E11–16:OAc) and its alcohol, (E)-11-hexadecenol (E11–16:OH), have been identified as major and minor sex pheromone components, respectively, few males were attracted to a blend of these compounds in Vietnamese fields. In order to utilize synthetic pheromone of L. orbonalis as a tool for sustainable pest management programs, we reexamined the pheromone of this species in order to search for other minor components. Gas chromatography-electroantennogram detection and gas chromatography/mass spectrometry analyses of abdominal tip extract revealed the presence of two electroantennogram-active compounds, E11–16:OAc and (3Z,6Z,9Z)-3,6,9-tricosatriene (Z3,Z6,Z9–23:H) in a ratio of 100:2. An extract of the abdomen and thorax showed an additional electroantennogram-active component, (3Z,6Z,9Z)-3,6,9-docosatriene (Z3,Z6,Z9–22:H), with the three compounds (E11–16:OAc, Z3,Z6,Z9–23:H and Z3,Z6,Z9–22:H) being present in a ratio of 100:45:1, indicating that the trienes were mainly present on the cuticular surface. In the field, traps baited with E11–16:OAc and the C23 triene, in a mix of 10:1, caught more male moths than traps baited with the acetate alone. A field evaluation of other polyunsaturated hydrocarbons showed that the C22 triene found in body extract also increased catches when added to the acetate, but no other hydrocarbons did. In contrast, to other studies with this moth, the addition of E11–16:OH to E11–16:OAc plus the C22 or C23 triene, resulted in decreased trap catches.

Female Sex Pheromone Secreted by Carmenta mimosa (Lepidoptera: Sesiidae), a Biological Control Agent for an Invasive Weed in Vietnam

Larvae of the clearwing moth, Carmenta mimosa (Lepidoptera: Sesiidae), bore into the trunk of Mimosa pigra L., which is one of the most invasive weeds in Vietnam. GC-EAD and GC-MS analyses of a pheromone gland extract revealed that the female moths produced (3Z,13Z)-3,13-octadecadienyl acetate. A lure baited with the synthetic acetate alone successfully attracted C. mimosa males in a field test. While the addition of a small amount of the corresponding alcohol did not strongly diminish the number of captured males, a trace of the aldehyde derivative or the (3E,13Z)-isomer markedly inhibited the attractiveness of the acetate. The diurnal males were mainly attracted from 6:00 am to 12:00 am.