A Sex Pheromone in the Desert Tenebrionid Beetle <Emphasis Type="Italic">Parastizopus armaticeps</Emphasis>

Males of the desert beetle Parastizopus armaticeps (Pér.) (Coleoptera: Tenebrionidae) exhibit a characteristic calling behavior that attracts females by raising the tip of the abdomen, exposing the aedeagus, and remaining in this posture for a few seconds while emitting a pheromone. We collected the pheromone by holding a solid phase microextraction fiber (100 mum polydimethylsiloxane) close to the aedeagus for 5 s and analyzed the volatiles collected by gas chromatography/mass spectrometry. The volatiles consisted of 3-methylphenol (52%), ethyl-1,4-benzoquinone (48%), and 3-ethylphenol (2%). The pheromone originated from the aedeagal glands. In the gland reservoirs, these compounds (2.1%) were mixed with ethyl, isopropyl, and propyl esters of fatty acids (24.2%), and a mixture of hydrocarbons (69.1%). The mean amount of volatiles extracted from gland reservoirs was 0.92 +/- 0.83 microg. Chemo-orientation experiments with a servosphere show that females responded only to the ternary volatile mixture. Females stopped walking, elevated the front parts of their bodies with erected antennae, turned slowly on their own axis, and walked upwind toward the odor source. Single components or binary mixtures did not elicit responses from females. Males did not respond to the pheromone. Evolutionary aspects of this pheromone system are discussed.     

A Novel Long-Chained Acetate in the Defensive Secretion of Thrips

Defensive secretions of adult and larval Suocerathrips linguis (Phlaeothripidae, Thysanoptera) were found to contain a long-chained acetate, (11Z)-11,19-eicosadienyl acetate, that was not previously known to occur naturally. This substance occurred together with octadecyl acetate and other long-chained acetates. The eicosadienyl acetate repels ants and spreads on the surface of such potential predators. The mixture can provide a long-lasting surface coating.     

Defensive secretion of the carabid beetlePasimachus subsulcatus

The defensive secretion of the carabid beetlePasimachus subsulcatus is a concentrated solution (up to 90%) of carboxylic acids, amounting to about 1% of body mass. It contains three major components (methacrylic, tiglic, and angelic acids) and four minor components (isobutyric, 2-methyl-butyric, isovaleric, and senecioic acids). In the single population of this large flightless beetle that was examined, the relative ratio of acidic components was remarkably constant from individual to individual.Report No. 87 of the series Defense Mechanisms of Arthropods; No. 86 is Dussourd, D., et al.,Proc. Natl. Acad. Sci. 85, 5992 (1988).     

Identification of (Z)-4-tridecene from Defensive Secretion of Green Lacewing, Chrysoperla carnea

We report the identification of a defensive secretion from the green lacewing, Chrysoperla carnea. By using combined gas chromatography–electroantennographic detection (GC-EAD), we found one major compound in the solvent extract of this secretion that elicited a significant EAD response from the antenna. Based upon its characteristic fragments from gas chromatography–mass spectrometry (GC-MS) analysis, the compound was identified as a tridecene. Dimethyldisulfide derivatization suggested that a double bond was located between positions 4 and 5 in the carbon chain. Thus, the compound was tentatively identified as a 4-tridecene. Coinjection of the extract with a mixture of the Z or E form of the synthetic 4-tridecene revealed that the unknown was (Z)-4-tridecene. EAG dose–responses showed a direct correlation to dose. Single sensillum recordings from sensilla trichodea situated on the antennae suggested the presence of receptor neurons specifically responding to this compound. An arrestment behavior was observed when tested in the Y-tube olfactometer. Preliminary field trapping results indicate that the compound is an antagonist to attraction. The avoidance behavior of predatory ants, observed when tested with the synthetic compound of this secretion further suggested a defensive function.     

Defensive secretion production in the tenebrionid beetle,Zophobas atratus

Beetles were milked of their abdominal defensive secretion at three different frequencies over the first 36 days of adult life. Secretion production decreased greatly with age from a maximum of 94 nmol/day at 4–6 days to a basal level of about 25 nmol/day at 30–40 days. Ethyl- and methylquinone comprised the bulk of the secretion and were most strongly affected by age. Benzoquinone was most strongly affected by milking frequency. An average adult produced an estimated 4445 nmol of total secretion in its 5-month life-span but had reservoirs large enough to store 11,000 nmol. Males produced more secretion than females because of their larger size and inherent sexual differences. As they aged, mated females showed a more rapid decrease in production that virgin females. The defensive system appears to be programed to charge glands rapidly with secretion early in adult life and fall of to a low recharge rate little affected by discharge.     

Kairomones for the egg parasiteTrichogramma evanescens Westwood

In observation-cage experiments some new contact kairomones for the egg parasiteTrichogramma evanescens Westwood are demonstrated.T. evanescens females search significantly longer on cabbage leaves treated with the wing scales of two hosts,Pieris brassicae L. andP. rapae L. Further, egg washes ofP. brassicae containing an oviposition deterrent pheromone for the butterflies, were found to have a contact-kairomonal effect on the parasite.T. evanescens females search significantly longer on cabbage leaves sprayed with a methanol or water wash ofP. brassicae eggs than on leaves treated with the solvent only.Hymenoptera: Trichogrammatidae.Lepidoptera: Pieridae.     

Defensive and pheromonal secretion of the tergal gland of Aleochara curtula

The defensive secretion from the tergal gland of the staphylinid beetle,Aleochara curtula, acting as a supplementary mating stimulant, was investigated by gas-liquid chromatography, mass spectrometry, and IR spectroscopy. The reservoir contains a complex mixture of hydrocarbons, aliphatic aldehydes, and substituted 1,4-benzoquinones.n-Undecane, 1-undecene, and (Z)-4-tridecene were identified as the major hydrocarbon components. The main aldehydes aren-dodecanal and (Z)-5-tetradecenal, and the chief quinones are toluquinone and 2-methoxy-3-methyl-1,4-benzoquinone, the latter being established structurally by comparison of the mass spectra of the three synthesized isomers. Quantitative GLC analyses revealed no sex specificity of the relative concentrations of the compounds.Coleoptera: Staphylinidae (Aleocharinae)     

Electrophysiological and Behavioral Responses of the Multicolored Asian Lady Beetle, <Emphasis Type="Italic">Harmonia axyridis</Emphasis> Pallas,to Sesquiterpene Semiochemicals

The role of two volatile sesquiterpenes, (E)-β-farnesene and (−)-β-caryophyllene, in the chemical ecology of the multicolored Asian lady beetle, Harmonia axyridis Pallas, was investigated by using both electrophysiological and behavioral techniques. (E)-β-Farnesene is the major component of the alarm pheromone of most aphid species, which are preyed on by H. axyridis. (−)-β-Caryophyllene was previously isolated from the headspace volatiles above overwintering and aggregated H. axyridis females. These sesquiterpenes elicited significant electroantennogram (EAG) activity from both H. axyridis male and female antennae. In a four-arm olfactometer, male and female H. axyridis were highly attracted toward (E)-β-farnesene, whereas only males were attracted to (−)-β-caryophyllene. In a bioassay technique that used a passively ventilated plastic box, both male and female H. axyridis aggregated in the (−)-β-caryophyllene-treated side of the box. These results support the potential usefulness of (E)-β-farnesene and (−)-β-caryophyllene in push–pull strategies that use H. axyridis as a biological control agent in aphid-infested sites or to control this new urban pest in residential structures.     

(Z)-7-Tricosene and Monounsaturated Ketones as Sex Pheromone Components of the Australian Guava Moth Coscinoptycha improbana: Identification, Field Trapping, and Phenology

Pheromone gland extracts of the Australian guava moth Coscinoptycha improbana (Lepidoptera: Carposinidae), contained four compounds that elicited responses from male moth antennae in gas chromatography-electroantennogram detection (GC-EAD) analyses. These were identified by GC-mass spectrometry as (Z)-7-tricosene (Z7-23Hy), (Z)-7-octadecen-11-one (Z7-11-one-18Hy), (Z)-7-nonadecen-11-one (Z7-11-one-19Hy), and (Z)-7-tricosen-11-one (Z7-11-one-23Hy) at a ratio of 65:23.5:1.5:10, respectively. Z7-23Hy, Z7-11-one-18Hy, and Z7-11-one-23Hy have not previously been reported as lepidopteran sex pheromone components. Z7-11-one-18Hy was active as a single component, and was synergized by Z7-11-one-23Hy but not Z7-11-one-19Hy, although the latter compound was weakly attractive as a single component. Addition of Z7-23Hy further increased attraction. The amount of the major pheromone component, Z7-11-one-18Hy in female pheromone gland extracts was estimated to be 16.4 ng/female (N = 8). Phenological data gathered over a 12-mo period in 2002 and 2003 using the binary blend indicated that moths are active throughout the year. The pheromone has already been employed to monitor the spread of C. improbana in New Zealand and detect its presence in Queensland, Australia.     

Attraction of Piezodorus hybneri to the Aggregation Pheromone Components of Riptortus clavatus

The aggregation pheromone of Riptortus clavatus (Heteroptera: Alydidae) consists of (E)-2-hexenyl (Z)-3-hexenoate (E2HZ3H), (E)-2-hexenyl (E)-2-hexenoate (E2HE2H), and myristyl isobutyrate (MI). Experiments were conducted to examine the attraction of Piezodorus hybneri (Heteroptera: Pentatomidae) to the pheromone components of R. clavatus, individually and in combination, and to determine if P. hybneri produces these compounds. Electroantennogram (EAG) responses of P. hybneri to E2HE2H were significant in a dose dependent manner, while those to E2HZ3H were not significantly different from those to hexane and air. Field trapping tests using E2HZ3H, E2HE2H, and MI, individually or in combination, showed that only E2HE2H was attractive to P. hybneri. E2HE2H was not detected in whole-body extracts or volatile collections from either sex of P. hybneri adults. We propose that the response of P. hybneri adults to the R. clavatus aggregation pheromone may be related to finding suitable host plants.     

Chemistry and Defensive Efficacy of Secretion of Burrowing Bug (Sehirus cinctus cinctus)

Adult Sehirus cinctus cinctus emit a volatile secretion from their metathoracic scent glands when tactually stimulated. We identified the volatile components by gas chromatography, high-performance liquid chromatography, and mass spectrometry. The secretion of both sexes contained (1R)-(+)--pinene, (1S)-(–)--pinene, -myrcene, (R)-(+)-limonene, and -terpinolene. Two additional compounds were found in only female secretions: (E)-2-hexenyl acetate and (E)-2-octenal. We also tested the defensive capability of this insect by offering it to various predators. Anoles, starlings, and a killdeer rejected S. c. cinctus after an initial sampling. These findings suggest that the secretion plays a defensive role.     

Host Plant Volatiles Synergize Response to Sex Pheromone in Codling Moth, Cydia pomonella

Plant volatile compounds synergize attraction of codling moth males Cydia pomonella to sex pheromone (E,E)-8,10-dodecadien-1-ol (codlemone). Several apple volatiles, known to elicit a strong antennal response, were tested in a wind tunnel. Two-component blends of 1 pg/min codlemone and 100 pg/min of either racemic linalool, (E)-beta-farnesene, or (Z)-3-hexen-1-ol attracted significantly more males to the source than codlemone alone (60, 58, 56, and 37%, respectively). In comparison, a blend of codlemone and a known pheromone synergist, dodecanol, attracted 56% of the males tested. Blends of pheromone and plant volatiles in a 1:100 ratio attracted more males than 1:1 or 1:10,000 blends. Adding two or four of the most active plant compounds to codlemone did not enhance attraction over blends of codlemone plus single-plant compounds. Of the test compounds, only farnesol was attractive by itself; at a release rate of 10,000 pg/min, 16% of the males arrived at the source. However, attraction to a 1:10,000 blend of codlemone and farnesol (42%) was not significantly different from attraction to codlemone alone (37%). In contrast, a codlemone mimic, (E)-10-dodecadien-1-ol, which attracted 2% males by itself, had a strong antagonistic effect when blended in a 1:10,000 ratio with codlemone.     

Optical resolution of (±)-Threo-9,10,16-trihydroxy hexadecanoic acid using (−)brucine

The optical resolution of (±)threo-9,10,16-trihydroxy hexadecanoic acid was achieved by fractional crystallization using (−)brucine. Formation of an estolide during decomposition of the (−)brucine complex was observed to interfere with the separation of the optically pure material. This was corrected by converting the estolide to (+)-threo-9,10,16-trihydroxy hexadecanoic acid via alcoholic alkaline hydrolysis followed by neutralization. Enantiomeric purity was determined by chiral lanthanide nuclear magnetic resonance shift reagent.     

Sex Pheromone Components of Indian Gypsy Moth, <Emphasis Type="Italic">Lymantria obfuscata</Emphasis>

The Indian gypsy moth, Lymantria obfuscata (Lepidoptera: Lymantriidae), has been recognized as a distinct species since 1865 but closely resembles a diminutive form of gypsy moth, Lymantria dispar. We tested the hypothesis that the sex pheromones of L. obfuscata and L. dispar are similar. In laboratory mate acceptance studies, very few male L. dispar made copulatory attempts when paired with female L. obfuscata, suggesting that female L. obfuscata emit one or more pheromone components antagonistic to male L. dispar. In coupled gas chromatographic–electroantennographic detection (GC–EAD) analyses of pheromone gland extract of female L. obfuscata, (Z)-2-methyloctadec-7-ene (2Me-7Z-18Hy) and (7R,8S)-cis-7,8-epoxy-2-methyloctadecane [(+)-disparlure] were most abundant and elicited the strongest responses from male L. obfuscata antennae. In field experiments near Solan (Himachal Pradesh, India), 2Me-7Z-18Hy and (+)-disparlure in combination attracted more male L. obfuscata than did either component alone. This two-component sex pheromone contrasts with the single-component sex pheromone [(+)-disparlure] of L. dispar. The contrasting composition of the lymantriid communities inhabited by L. obfuscata and L. dispar may explain why 2Me-7Z-18Hy is a pheromone component in L. obfuscata and a pheromone antagonist in L. dispar and why (−)-disparlure reduces pheromonal attraction of male L. dispar but not male L. obfuscata.     

Defensive secretion of chrysomelid larvaeLinaeidea aenea linné andPlagiodera versicolora distincta Baly

The larval defensive secretions ofLinaeidea aenea Linné andPlagiodera versicolora distincta Baly were identified as plagiolactone and epiplagiolactone. In addition to these compounds, chrysomelidial and the acetates of hexadecanol, octadecanol and (Z)-I 1-eicosenol from the former insect, and plagiodial and epichrysomelidial from latter insect were identified.This is report No. 3 of the Defensive Secretion of Chrysomelid Beetles. Report No. 2 is Sugawara et al., 1979.     

Green leaf volatiles as antiaggregants for the mountain pine beetle,Dendroctonus ponderosae Hopkins (Coleoptera: Scolytidae)

We tested the hypothesis that green leaf volatiles act as antiaggregants for the mountain pine beetle (MPB),Dendroctonus ponderosac Hopkins. In coupled gas chromatographic-electroantennographic detection (GC-EAD) analysis MPB antennae responded to 30 ng doses of all six-carbon green leaf alcohols tested [1-hexanol, (E)-2-hexen-1-ol, (Z)-2-hexen-1-ol, (E)-3-hexen-1-ol, and (Z)-3-hexen-1-ol], but not to the aldehydes, hexanal or (E)-2-hexenal, or to alcohol or aldehyde homologues with more or fewer than six carbon atoms. In field trapping experiments a blend of green leaf alcohols [1-hexanol, (Z)-2-hexen-1-ol, (E)-3-hexen-1-ol and (Z)-3-hexen-1-ol] effectively disrupted the response to attractive semiochemicals; a blend of the aldehydes hexanal and (E)-2-hexenal was inactive. The two best disruptants. (E)-2-hexen-1-ol and (Z)-3-hexen-1-ol, reduced catches of both sexes to levels not significantly different from catches in unbaited control traps. They also reduced the attack on trees baited with attractive MBP pheromones to a level not significantly different from that on unbaited control trees. Neither of the clerid predators captured,Enoclerus sphegeus (F.) norThanasimus undatulus (Say), was repelled by green leaf volatiles. Our results suggest that green leaf alcohols are promising disruptants which may be used to supplement the antiaggregation pheromone, verbenone, in protecting single high-value trees as well as carefully selected stands with low-level populations of MPBs.     

Sequestration of Host Plant Glucosinolates in the Defensive Hemolymph of the Sawfly Athalia rosae

Interactions between insects and glucosinolate-containing plant species have been investigated for a long time. Although the glucosinolate–myrosinase system is believed to act as a defense mechanism against generalist herbivores and fungi, several specialist insects use these secondary metabolites for host plant finding and acceptance and can handle them physiologically. However, sequestration of glucosinolates in specialist herbivores has been less well studied. Larvae of the turnip sawfly Athalia rosae feed on several glucosinolate-containing plant species. When larvae are disturbed by antagonists, they release one or more small droplets of hemolymph from their integument. This reflex bleeding is used as a defense mechanism. Specific glucosinolate analysis, by conversion to desulfoglucosinolates and analysis of these by high-performance liquid chromatography coupled to diode array UV spectroscopy and mass spectrometry, revealed that larvae incorporate and concentrate the plant's characteristic glucosinolates from their hosts. Extracts of larvae that were reared on Sinapis alba contained sinalbin, even when the larvae were first starved for 22 hr and, thus, had empty guts. Hemolymph was analyzed from larvae that were reared on either S. alba, Brassica nigra, or Barbarea stricta. Leaves were analyzed from the same plants the larvae had fed on. Sinalbin (from S. alba), sinigrin (B. nigra), or glucobarbarin and glucobrassicin (B. stricta) were present in leaves in concentrations less than 1 mol/g fresh weight, while the same glucosinolates could be detected in the larvae's hemolymph in concentrations between 10 and 31 mol/g fresh weight, except that glucobrassicin was present only as a trace. In larval feces, only trace amounts of glucosinolates (sinalbin and sinigrin) could be detected. The glucosinolates were likewise found in freshly emerged adults, showing that the sequestered phytochemicals were transferred through the pupal stage.     

Alkadienes and Alkenes, Sex Pheromone Components of the Almond Seed Wasp Eurytoma amygdali

Whole body extracts of virgin Eurytoma amygdali females were attractive to males in laboratory bioassays. Extracts of various body parts of the female wasp elicited different responses to males, with the thorax extract being the most active. Preparative fractionation of the crude hydrocarbon extract on a silver nitrate impregnated silica gel column (alkanes, alkenes, and alkadienes) revealed that the highest male response was elicited by alkadienes and the lowest by alkenes, with the alkane fraction being inactive. The identification of alkenes and alkadienes was based on gas chromatographic, mass spectrometric, and gas-phase infrared data. Laboratory bioassays suggested that the two alkadienes, (Z,Z)-6,9-tricosadiene [(Z,Z)-6,9-C_23:2], and (Z,Z)-6,9-pentacosadiene [(Z,Z)-6,9-C_25:2], and to a lesser extent alkenes, identified in the female extract of E. amygdali were male attractants.     

Defense Secretion of Prorhinotermes simplex: Toxicity to Insecticide Susceptible and Resistant House Fly

(E)-1-Nitropentadec-1-ene (NPE), the main component of the defense secretion of Prorhinotermes simplex soldiers, is toxic to both insecticide-susceptible (S) as well as to insecticide-resistant (R) strains of the house fly, Musca domestica. The LD₅₀ is 11.7 g/female fly for the S strain and 9.7 g for the R strain. The same efficacy of NPE on R and S strains indicates a different mechanism of action compared to conventional chlorinated, organophosphorus, and pyrethroid insecticides. Termite nestmates are protected against NPE by a specific detoxification mechanism. 1-Nitropentadecane, the detoxification product of NPE is nearly nontoxic to house flies, and doses up to 160 g/fly caused only very low mortality.     

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.