Macrocyclic lactones and isopentenyl esters in the Dufour's gland secretion of halictine bees (Hymenoptera: Halictidae)

The volatile components of the Dufour's gland secretion of female halictid bees have been examined in 18 Nearctic species belonging toAgapostemon, Augochlora, Augochlorella, Augochloropsis, Dialictus, Evylaeus, Halictus, andLasioglossum. Nine saturated and unsaturated macrocyclic lactones ranging from C₁₈ to C₂₆ have been identified. Four of these compounds, the saturated C₂₆ and the unsaturated C₂₀, C₂₂, and C₂₄ lactones, are new natural products reported for halictine bees. A series of eight esters containing branched C₅-alkenols and fatty acids has been identified in several species. The cell linings and pollen ball inAugochlora pura pura contain the same major lactones as the Dufour's gland. A discussion of the significance of the Dufour's gland secretion for apoid systematics and its function in the Halictidae is presented.     

Species,individual and kin specific blends in Dufour's gland secretions of halictine bees

The compositions of Dufour's gland secretions of four sympatric halictine bee species were chemically studied by combined gas chromatography-mass spectrometry. The secretion is composed of C₁₆-C₂₄ macrocyclic lactones, isopentenyl esters, and hydrocarbons. Comparative analyses have revealed that the blends of compounds are species specific. Studies of individual glands belonging to bees of the speciesEvylaeus malachurum have demonstrated that each bee exhibits a specific blend in its Dufour's gland. Nestmate bees (considered as sister bees), however, are more similar to each other than nonrelated bees. The relative importance of species specificity, individual specificity, and similarities between kins are discussed.     

Trail pheromone of ponerine ant Gnamptogenys striatula: 4-methylgeranyl esters from Dufour's gland

Dufour's gland is the origin of the trail pheromone of Gnamptogenys striatula. Chemical analysis of the glandular extracts revealed a series of new natural products, especially esters of (2E)-3,4,7-trimethyl-2,6-octadien-1-ol (4-methylgeraniol), and (2E)-3,4,7-trimethyl-2,6-nonadien-1-ol (a bishomogeraniol isomer) with medium-chain fatty acids. Bioassays with synthetic racemates of the esters revealed that the 4-methylgeranyl esters are highly active as trail pheromones, while the bishomogeranyl esters are either marginally active or not active at all. Assays with the individual 4-methylgeranyl esters showed each of them to be inferior to the glandular secretion in eliciting trail following. However, the mixture of racemic 4-methylgeranyl octanoate and the corresponding decanoate and dodecanoate, the main Dufour's volatile constituents, is as active as the natural secretion at similar concentration. We conclude that the trail pheromone constitutes a mixture of at least the 4-methylgeranyl esters identified in the gland. Since G. striatula generally preys on small arthropods rather than monopolizing large resources, we assume that trails are rarely used during foraging, but more often during nest migration. Production of new societies in this species is generally performed by budding, a period of considerable predation risk. Utilizing trails for efficient displacement in this context is, therefore, highly adaptive. This behavioral repertoire may also provide the ants with additional means of food resource exploitation.     

Chemistry of the Dufour's gland secretions of North American andrenid bees (Hymenoptera: Andrenidae)

The volatile components of the Dufour's gland secretions were examined in 22 Nearctic species of andrenid bees representing 10 subgenera. Farnesyl hexanoate was the dominant component in the secretion of 17 species. In others, various terpenoid esters such as geranyl octanoate, farnesyl octanoate and geranylgeranyl octanoate were the major components. Approximately 30 compounds have been identified in the secretions; many are newly identified in andrenid bees. Three different groups of secretions are discerned with exceptions. A discussion of the possible function of the Dufour's gland secretion in the biology of, and its use in, the systematics of these bees is presented.     

Biochemical and behavioral evidence foe hybridization between fire ants,Solenopsis invicta andSolenopsis richteri (Hymenoptera: Formicidae)

Behavioral and biochemical evidence is presented for hybridization between the fire ants,Solenopsis richteri andS. invicta. The response of the two species to extracts of their trail pheromones presented as a point source is clearly species-specific; however, hybrid workers responded to parental Dufour's gland extracts and parental workers responded to Dufour's gland extracts of the hybrid. The behavioral evidence for hybridization was confirmed by gas Chromatograph comparison of the Dufour's gland extracts of the three fire ant forms, which showed a pattern for the hybrid that was intermediate to the two parental species.     

Volatile hydrocarbons in the dufour's gland of the parasiteNemeritis canescens (Grav.) (Hymenoptera; ichneumonidae)

The Dufour's gland of the parasitic waspNemeritis (= Venturia) canescens (Grav.) was shown by gas chromatography and mass spectrometry to contain a mixture of C₂₁, C₂₃, and C₂₅ saturated and monounsaturated hydrocarbons. The main component (62%) was (Z)-10-tricosene. The biological activity of the components is discussed.     

Volatile Components in Dorsal Gland Secretions of the White-Lipped Peccary, Tayassu pecari, from Bolivia

Secretions from the dorsal gland of male and female free-ranging adult white-lipped peccaries (Tayassu pecari) from Bolivia were analyzed by gas chromatography–mass spectrometry. Fifty compounds were identified, some provisionally. Secretions of both sexes contain saturated and unsaturated C₅–C₁₈ carboxylic acids as well as isomers of the diterpene springene. The females' secretions uniquely possess farnesyl esters of C₈ and C₁₀ carboxylic acids, whereas the males' secretions uniquely showed two compounds provisionally identified as monounsaturated C₁₆ lactones. Saturated high-molecular-weight esters of C₁₀ carboxylic acids are more abundant in the females' secretions than in those of the males. The secretions of both sexes also contain monoalkanoate esters of methylhydroquinone as major components.     

Isolation,identification, and function of the Dufour gland secretion ofXylocopa virginica texana (Hymenoptera: Anthophoridae)

The Dufour's gland secretion ofXylocopa virginica texana possesses short-term repellency for conspecifics when applied to passion flowers. This secretion contains a number of straight-chain hydrocarbons. The two major components are the methyl esters of palmitic and myristic acid. A mixture of the two esters and two of the available hydrocarbons were as effective as the Dufour's gland extract in eliciting a response in females to the passion flower,Passiflora incarnata, to which the extract was applied.Approved as TA13387 by the Director, Texas Agricultural Experiment Station and conducted in cooperation with the USDA. Supported in part by NSF-DEB-76-03963.     

Host recognition and the study of a chemical basis for attraction by cuckoo bumble bees (Hymenoptera: Apidae)

Species ofPsithyrus (Hymenoptera; Apidae) are obligate bumble bee social parasites. In this study, females ofP. vestalis andP. ashtoni were presented with pentane extracts prepared from different body parts of queens of their respective host species,Bombus terrestris andB. terricola. Parasites of both species were capable of distinguishing host bees from other bumble bee species using chemical cues contained within extracts. Among extracts of several body parts presented to parasites, the abdomen produced the greatest behavioral response, with Dufour's gland and terminal tergal segments eliciting the greatest response among abdominal regions. Extracts of these two body parts obtained fromB. terrestris queens shared a number of compounds, identified by GC-MS. Among the identified compounds are a number that have been reported to be of importance in bee sociochemistry.     

Odor correspondence betweenMelitta females and males of their nest parasiteNomada flavopicta K. (Hymenoptera: Apoidea)

Analyses have been performed with the help of combined capillary gas chromatography and mass spectrometry on volatile secretions emanating from the Dufour glands of femaleMelitta haemorrhoidalis andM. leporina and heads of maleNomada flavopicta, a nest parasite of theMelitta species. It was found that the cephalic secretions ofN. flavopicta males have definite similarities with the Dufour gland secretions of the two species ofMelitta. They all contain octadecyl butyrate as a major component. Monounsaturated alcohols of different chain lengths are also present in the secretions. Beside these compounds,Melitta has some other esters, notably C₁₂-, C₁₄-, C₁₆-, and C₂₀-butyrates as well as C₁₂- and C₁₆-acetates.     

Identification and bioassay of macrocyclic lactone sex pheromone of the halictine beeLasioglossum zephyrum

The macrocyclic lactones found in the Dufour's gland of the halictine beeLasioglossum zephyrum are female sex pheromones. Octadecanolide, eicosanolide, docosanolide, and tetracosanolide, as well as monounsaturated homologs of each, are components of the Dufour's gland secretion of this species. Furthermore, a series of odd-carbon-numbered saturated and unsaturated hydrocarbons and isopentenyl docosanoate occur in extracts of the Dufour's gland and of whole females. Two different mixtures of all four synthetic lactones, and additionally a treatment consisting of the natural extract, elicit higher response levels than two of the lactones separately or either of the controls.     

Identification of new homoterpene esters from Dufour's gland of the ponerine ant Gnamptogenys striatula

Extracts of Dufour's gland of the ponerine ant, Gnamptogenys striatula, were analyzed by using the combination of gas chromatography and mass spectrometry. Series of esters of the new homoterpenoids (2E,6)-3,4,7-trimethyl-2,6-octadiene-1-ol (4-methylgeraniol) and (2E,6)-3,4,7-trimethyl-2, 6-nonadiene-1-ol (bishomogeraniol) with unbranched medium-chain fatty acids were identified. Transformation of the chiral natural products into 1,4-di(trifluoroacetoxy)-3-methylpentane and comparison of its gas chromatographic retention time on a modified cyclodextrin phase with that of synthetic optically active reference samples proved the stereogenic center to keep (S)-configuration. (2E,4S,6)-3,4,7-Trimethyl-2,6-octadien-1-yl decanoate and the corresponding dodecanoate are the main volatiles in the extracts.     

Surface Properties and Biological Activity of Select Cationic Surfactants

A series of cationic surfactants, N-(decyl N-tri-ethanol ammonium Bromide) (C₁₀), N-(dodecyl N-triethanol ammonium Bromide) (C₁₂), N-(hexadecyl N-triethanol ammonium Bromide) (C₁₆) were synthesized. These compounds have been evaluated by studying their surface properties, surface parameters, biodegradability and antimicrobial and antifungal activities.

A comparative study of the exocrine products of cleptoparasitic bees (Holcopasites) and their hosts (Calliopsis) (Hymenoptera: Anthophoridae,Andrenidae)

The cephalic secretion of females of the cleptoparasitic beeHolcopasites calliopsidis contains two main volatiles, 6-methyl-5-hepten-2-one and geranyl acetone. The mandibular gland secretion of its host,Calliopsis andreniformis, on the other hand, contains the two isomeric forms of citral (neral and geranial). Neral and geranial are also produced by mandibular glands of two other species ofCalliopsis and one species in the related genusNomadopsis. The Dufour's gland ofC. andreniformis contains an oily secretion composed of hydrocarbons that are deposited on the brood cell walls and pollen balls providing a waterproof lining for both.     

Isolation of the trail recruitment pheromone ofSolenopsis invicta

TheSolenopsis invicta trail pheromone is synthesized by the Dufour's gland and is released through the sting apparatus. The recruitment subcategory of theS. invicta trail pheromone was shown to be composed of a mixture of the orientation pheromone, (Z,E)--farnesene and an unidentified homosesquiterpene consisting of three rings and one double bond (C-1). C-1 is present in worker Dufour's glands at only 75 pg per worker equivalent. This is the first report that demonstrates that different exocrine products from the same gland control different subcategories of behavior related to mass recruitment.     

Sponge fatty acids. 3. Occurrence of series of n−7 monoenoic andiso-5,9 dienoic long-chain fatty acids in the phospholipids of the marine spongeCinachyrella aff.schulzei keller

The fatty acid composition of phospholipids from the New Caledonian spongeCinachyrella aff.schulzei Keller was studied. More than 60 fatty acids were identified as methyl esters andN-acyl pyrrolidides by gas chromatography and gas chromatography/mass spectrometry. Two isoprenoid fatty acids also were shown to be present, namely 4,8,12-trimethyltridecanoic and 5,9,13-trimethyltetradecanoic acids. The unusual 6-tetradecenoic, 6-pentadecenoic, 12-nonadecenoic and 26-methylheptacosanoic (iso-28∶0) acids were found for the first time in sponge phospholipids. A series of six n−7 monoenoic long-chain fatty acids (C₂₃ to C₂₈) were identified, including the rare 16-tricosenoic, 18-pentacosenoic and 21-octacosenoic acids. Fifteen fatty acids possessing the typical 5,9 dienoic moiety accounted for 30% of the total fatty acid mixture. Two new fatty acids were identified, namely 5(Z)-octacosenoic and 27-methyl-5(Z),9(Z)-octacosadienoic (iso-5,9-29∶2). Based on gas chromatography/Fourier transform infrared experiments, the double bonds were assigned the (Z) configuration. For part 2 of this series, see Reference 1.     

Pheromones of two arctiid moths (Creatonotos transiens andC. gangis)

The two major components of the female sex pheromones of twoCreatonotos species have been identified as an achiral C₂₁ triene, (Z,Z,Z)-3,6,9-heneicosatriene, and a chiral epoxide, (Z,Z)-2(2,5-octadienyl)-3-undecyloxirane. The ratios of these components in the two species fall into nonoverlapping ranges. Two additional achiral minor components, (Z,Z)-6,9-heneicosadiene and (Z,Z,Z)-3,6,9-tricosatriene, were also identified in the female sex gland extracts. The male pheromone of both species consists of hydroxydanaidal, a chiral dihydropyrrolizine derived from pyrrolizidine alkaloids in the larval diet.Creatonotos transiens was found to convert dietary heliotrine into (R)-(–)-hydroxydanaidal, with inversion at the single asymmetric carbon atom. The possible biological and biosynthetic significance of the chiral pheromone components are discussed, and they are compared with known examples of chiral lepidopteran pheromones.     

Secondary amines isolated from venom gland of dolichoderine antTechnomyrmex albipes

A series of unsaturated secondary amines have been isolated from the dolichoderine antTechnomyrmex albipes (F. Smith). The major components of the mixture have been shown by spectroscopic procedures to be dinon-8-enylamine, andN-hept-6-enylnon-8-enamine, and these structural assignments have been confirmed by synthesis. Mass spectrometry indicates the presence of trace amounts of the bis C₁₁ amine and the C₉-C₁₁ amine. The four amines, present in total at approximately 2.8g/ant, are located in the gaster of the insect in a gland that is considered to be the venom gland although it is atypical from a morphological standpoint.     

Identification, Synthesis, and Field Evaluation of the Sex Pheromone from the Citrus Leafminer, Phyllocnistis citrella

Using male antenna as the sensing element, three electroantennographic detection (EAD)-active peaks were detected from pheromone gland extracts of the citrus leafminer, Phyllocnistis citrella. Based on gas chromatography (GC)-mass spectrometry and GC-infrared data, the semiochemicals were tentatively identified as a novel pheromone, (Z,Z,E)-7,11,13-hexadecatrienal, a previously identified attractant, (Z,Z)-7,11-hexadecadienal, and (Z)-7-hexadecenal in a ratio of 30:10:1, respectively. Identification was confirmed with synthetic compounds, which gave retention times identical to those of the natural products on three capillary columns with polar and nonpolar phases. While traps baited only with the previously identified attractant alone did not catch any males in Brazil, binary and tertiary mixtures with the major constituents caught significantly more male moths than traps baited with five virgin females. This paper and the following paper (Moreira et al.) were submitted within a few days of each other. The editors and the authors agreed that they should be published in tandem.