Comparison of Age-dependent Quantitative Changes in the Male Labial Gland Secretion of <Emphasis Type="Italic">Bombus Terrestris</Emphasis> and <Emphasis Type="Italic">Bombus Lucorum</Emphasis>

Age-related changes of antennal-active components of male labial gland extracts were studied in two closely related bumblebee species, Bombus terrestris and B. lucorum. In B. terrestris, compounds eliciting electroantennogram (EAG) responses of virgin queens were ethyl dodecanoate, 2,3-dihydrofarnesal, 2,3-dihydrofarnesol, hexadecan-1-ol, octadeca-9,12,15-trien-1-ol, and geranylcitronellol. Compounds that elicited EAG responses from queens of B. lucorum were ethyl dodecanoate, ethyl tetradec-7-enoate, ethyl tetradec-9-enoate, ethyl hexadec-9-enoate, hexadecan-1-ol, hexadec-7-enal, octadeca-9,12-dien-1-ol, octadeca-9,12,15-trien-1-ol, and octadecan-1-ol. Quantities of these compounds in the labial glands changed significantly over the lifetime of the respective males of the two species. In both species, concentrations of the respective compounds reached their maximum within seven days after eclosion. Subsequently, a rapid decrease in the amount of EAG-active compounds occurred in B. terrestris, whereas in B. lucorum the amount of active compounds stayed approximately constant or decreased at a slow rate. Microscopy showed that in B. terrestris secretory cells of the labial glands undergo apoptosis from the fifth to the tenth day of life, whilst in B. lucorum labial gland cells remain unchanged throughout the life of the males.     

Identification of volatile sex pheromone components released by the southern armyworm,Spodoptera eridania (Cramer)

Analysis of sex pheromone gland extracts and volatile pheromone components collected from the calling female southern armyworm,Spodoptera eridania (Cramer), by high-resolution capillary gas chromatography and mass spectroscopy indicated that a number of 14-carbon mono- and diunsaturated acetates and a monounsaturated 16-carbon acetate were produced. Gland extracts also indicated the presence of (Z)-9-tetradecen-1-ol. However, this compound was not found in collections of volatiles. Field trapping studies indicated that the volatile blend composed of (Z)-9-tetradecen-1-ol acetate (60%), (Z)-9-(E)-12-tetradecadien-1-ol acetate (17%), (Z)-9-(Z)-12-tetradecadien-1-ol acetate (15%), (Z)-9-(E)-11-tetradecadien-1-ol acetate (5%), and (Z)-11-hexadecen-1-ol acetate (3 %) was an effective trap bait for males of this species. The addition of (Z)-9-tetradecen-1-ol to the acetate blends tested resulted in the capture of beet armyworm,S. exigua (Hubner), males which provides further evidence that the alcohol is a pheromone component of this species.     

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.     

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.     

Tracing Pollinator Footprints on Natural Flowers

Many insects are known to leave lipid footprints while walking on smooth surfaces. Presumably, the deposited substances improve tarsal adhesion. In bumblebees, footprint hydrocarbons also function as scent marks that allow detection and avoidance of recently depleted flowers. I used GC-MS to detect hydrocarbons deposited by bumblebee (Bombus pascuorum) on flowers of Lamium maculatum. In addition to the plants' own cuticular lipids, extracts of corollas that had been visited by bumblebees contained odd-numbered alkenes. The amount of pentacosenes (C₂₅H₅₀) on corollas was linearly related to the number of bumblebee visits, with workers depositing approximately 16 ng per visit (extrapolated to a total of 65 ng of bumblebee cuticular hydrocarbons). Pentacosenes were retained on visited flowers without loss for 2 hr, and probably longer. This and results from flight cage experiments suggest that flower epicuticles retain a chemical record of pollinator visitation, including information on visiting bee species. Continuous footprint accumulation necessitates new explanations concerning the reversibility of “repellent scent marks” of bumblebees.     

Premating Behavior of Bombus Confusus Males and Analysis of Their Labial Gland Secretion

Premating behavior in the bumblebee Bombus confusus was studied. Visual searching for females is not the only premating strategy of this species, as was believed earlier. Males of B. confusus have a normally developed labial gland and its secretion is used to mark a perch from which they visually search for females. The labial gland secretion contains geranylcitronellol and (Z)-9-octadecenyl acetate as the main components.     

Sex pheromone of fall armyworm,Spodoptera frugiperda (J.E. Smith)

Analyses of extracts of pheromone glands and of volatiles from calling female fall armyworm moths,Spodoptera frugiperda (J.E. Smith), revealed the presence of the following compounds: dodecan-1-ol acetate, (Z)-7-dodecen-1-ol acetate, 11-dodecen-1-ol acetate, (Z)-9-tetradecenal, (Z)-9-tetradecen-1-ol acetate, (Z)-11-hexadecenal, and (Z)-11-hexadecen-1-ol acetate. The volatiles emitted by calling females differed from the gland extract in that the two aldehydes were absent. Field tests were conducted with sticky traps baited with rubber septa formulated to release blends with the same component ratios as those emitted by calling females. These tests demonstrated that both (Z)-7-dodecen-1-ol acetate and (Z)-9-tetradecen-1-ol acetate are required for optimum activity and that this blend is a significantly better lure than either virgin females or 25 mg of (Z)-9-dodecen-1-ol acetate in a polyethylene vial, the previously used standard. Addition of the other three acetates found in the volatiles did not significantly increase the effectiveness of the two-component blend as a bait for Pherocon 1C or International Pheromones moth traps.Mention of a commercial or proprietary product does not constitute an endorsement by the USDA.     

Female sex pheromone of the pickleworm,Diaphania nitidalis (Lepidoptera: Pyralidae)

Heptane extracts of the ovipositors from pickleworm adults (Diaphania nitidalis) were found to contain (E)-11-hexadecenal along with proportionally smaller amounts of (Z)-11-hexadecenal, (E)- and (Z)-11-hexadecen-1-ol, hexadecanol, hexadecanal, and a trace amount of (E,Z)-10,12-hexadecadienal. Assays conducted in a flight tunnel and in the field showed that a synthetic mixture of the five unsaturated compounds elicited behavioral responses from pickleworm males that were indistinguishable from those elicited by extracts of the female or by mate-calling females. When any component was deleted from the set of five unsaturated compounds, the intensity and extent of male responses to the resulting mixtures were significantly attenuated. The female sex pheromone of the pickleworm resembles the pheromone of a congeneric species,D. hyalinata, but bioassays indicated that (E,E)-10,12-hexadecadienal, produced byD. hyalinata but not by the pickleworm, plays a role in pheromonal specificity.     

Specificity of the pheromone system ofAdoxophyes orana andClepsis spectrana

The pheromone system of the summer fruit tortrix mothAdoxophyes orana (Fischer von Röslerstamm) consists of a mixture ofcis-9- andcis-11-tetradecen-1-ol acetate (cis-9- andcis-11-TDA, respectively) in a ratio of 9:1. Substitution of one or both of these compounds by related unsaturated acetates reduced the attractancy. Onlycis-11-TDA could be replaced bycis-11-tridecen-1-ol acetate (cis-11-TriDA), although the 9:1 mixture ofcis-9-TDA andcis-11-TriDA was less attractive in the field than the pheromone system itself. The major component of the pheromone system of the leaf rollerClepsis spectrana (Treitschke)(cis-9-TDA:cis-11-TDA=1:9) could also be replaced bycis-11-TriDA, again with some reduction in attractancy.     

Identity and Function of Scent Marks Deposited by Foraging Bumblebees

Foraging bumblebees can detect scents left on flowers by previous bumblebee visitors and hence avoid flowers that have been depleted of nectar. Tarsal secretions are probably responsible for this repellent effect. The chemical components of the tarsal glands were analyzed by combined gas chromatography–mass spectrometry for three species of bumblebee, Bombus terrestris, B. lapidarius, and B. pascuorum. The hydrocarbons identified were similar for each species, although there were interspecific differences in the relative amounts of each compound present. The tarsal extracts of all three species comprised complex mixtures of long-chain alkanes and alkenes with between 21 and 29 carbon atoms. When B. terrestris tarsal extracts were applied to flowers and offered to foraging bumblebees of the three species, each exhibited a similar response; concentrated solutions produced a repellent effect, which decreased as the concentration declined. We bioassayed synthetic tricosane (one of the compounds found in the tarsal extracts) at a range of doses to determine whether it gave a similar response. Doses 10^–12 ng/flower resulted in rejection by foraging B. lapidarius. Only when 10^–14 ng was applied did the repellent effect fade. We bioassayed four other synthetic compounds found in tarsal extracts and a mixture of all five compounds to determine which were important in inducing a repellent effect in B. lapidarius workers. All induced repellency but the strength of the response varied; heneicosane was most repellent while tricosene was least repellent. These findings are discussed in relation to previous studies that found that tarsal scent marks were attractive rather than repellent.     

Sex pheromone of female african white rice stem borer,Maliarpha separatella (Lepidoptera: Pyralidae) from Sierra Leone: Identification and field testing

Analysis of ovipositor washings of femaleMaliarpha separatella from Sierra Leone by high-resolution gas chromatography (GC) linked to a male electroantennograph (EAG) indicated the presence of three electrophysiologically active compounds. The GC retention times of these compounds were consistent with those of (Z)-9-tetradecen-1-ol, (Z,E)-9,12-tetradecadien-1-ol, and (E,E)-10,12-tetradecadien-1-ol. Analysis by El and CI mass spectrometry of ovipositor washings confirmed these identifications and also indicated the presence of the saturated analog, tetradecan-1-ol. There was no evidence, from these analyses, of the corresponding aldehydes or acetates. The EAG-active compounds were present in the ovipositor washings in a ratio of approximately 23.51, with the major component constituting approximately 0.4 ng per ovipositor. GC-MS analysis of entrained female effluvia confirmed that the EAG-active compounds were released by virgin females. Field testing of the EAG-active compounds indicated that (Z,E)-9,12-tetradecadien-1-ol and (E,E)10,12-tetradecadien-1-ol were attractive to male moths in ratios of between 9:1 and 39:1, while (Z)-9-tetradecen-1-ol was found to reduce trap catch when added to blends of the other two compounds.     

Identification of sex pheromone components of darksided cutworm,Euxoa messoria,and modification of sex attractant blend for adult males

Eleven pheromone-like compounds were identified in excised abdomen tip extracts of calling adult females of darksided cutworm,Euxoa messoria (Harris). The essential pheromone components were (Z)-7- and (Z)-11-hexadecenyl acetates in a ratio of 140, which agreed with an attractant blend developed empirically by field testing the attractancies of synthetic blends. The pheromone component, (Z)-11-hexadecenol, improved the attraction of darksided cutworm males whereas the components (Z)-9-tetradecenyl acetate and (Z)-7-dodecenyl acetate inhibited their attraction. The other pheromone-like compounds identified in the female extracts had no obvious effect on the attraction of darksided cutworm males. Three compounds that functioned as parapheromones when substituted for (Z)-7-hexadecenyl acetate in the two-component blend were (Z)-7-pentadecenyl, (Z)-7-tetradecenyl, and (Z)-7-tridecenyl acetates. (Z)-11-hexadecenal was not detected in the female extracts, but it had a synergistic effect on the attraction of darksided cutworm moths and inhibited the attraction of male moths of a nontarget species,Helotropha reniformis (Grote). As a trap bait for monitoring purposes, we recommend a four-component blend of (Z)-7-hexadecenyl acetate, (Z)-11-hexadecenyl acetate, (Z)-11-hexadecenol, and (Z)-11-hexadecenal at 12.5, 500, 1, and 10 g/red rubber septum dispenser containing 5 g of antioxidant 2,6-tert-butyl-4-methyl phenol. This blend is effective under field conditions for at least six weeks.     

Scent Marking, Scent Origin, and Species Specificity in Male Premating Behavior of Two Scandinavian Bumblebees

The marking behavior and the scent-marking compounds in males of two Scandinavian bumblebee species Bombus pratorum and Bombus lapidarius were studied. There are characteristic differences in the behavior and in the chemistry of the two species. Males of B. pratorum scent marked small areas of the edges of birch leaves in a quick and unpredictable manner, depositing farnesol, geranylgeranyl acetate, farnesyl acetate, (Z)-11-octadecanol, hexadecanol, and a pentacosadiene. In B. lapidarius, scent marking on birch leaves was much slower and the entire edge of the leaf was marked with (Z)-9-hexadecenol and hexadecanol. These compounds were also detected in the cephalic portion of the labial gland in males. Thus, males of B. lapidarius produce a blend of fatty acid derivatives while B. pratorum males, in addition to fatty acid derivatives, also produce sesqui- and diterpenes. The total amount of scent compounds per milligram of labial glands was 0.2 μg in B. pratorum and 40 μg in B. lapidarius. Farnesol and farnesyl acetate were detected via headspace collection in the air around leaves marked by B. pratorum and (Z)-9-hexadecenol was detected around leaves marked by B. lapidarius.     

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.     

Sex pheromone of femaleMyelois cribrella Hübner (Lepidoptera: Pyralidae)

Females ofMyelois cribrella contain about 20 ng/gland of the primary sex pheromone components (Z)-9-tetradecenyl acetate, (9Z,12E)-9,12-tetradecadienyl acetate, and (Z)-11-hexadecenyl acetate in proportions of 4115, respectively. These physiologically active components are accompanied by a number of related compounds such as (Z)-9-tetradecen-1-ol, hexadecyl acetate, (9Z,12E)-9,12-tetradecadien-1-ol, (Z)-11-hexadecen-1-ol, octadecyl acetate, octadecan-1-ol, and eicosyl and docosyl acetates. Octadecyl acetate, the most abundant component, represents about 42 ng/female moth; however, no physiological activity could be attributed to it. In field tests, a trap baited with a 1-mg mixture of (Z)-9-tetradecenyl acetate, (9Z,12E)-9,12-tetradecadienyl acetate, and (Z)-11-hexadecenyl acetate in a ratio of 121 caught more male moths than three live female moths.Pheromones, 58. Pheromones, 57: Bestmann et al. (1987).     

Sex pheromone components of the variegated leafroller moth,Platynota flavedana

Female tip extracts of the variegated leafroller moth,Platynota flavedana (Clemens), were analyzed and found to contain a mixture of (E)-11-tetradecen-1-ol and (Z)-11-tetradecen-1-ol (91), as well as a mixture of (E)-11-tetradecenyl acetate and (Z)-11-tetradecenyl acetate (2-31). Small amounts of tetradecen-1-ol and tetradecyl acetate probably are also present. In the field, a mixture of the two alcohols (8416,EZ ratio) attracted significantly more male moths of this species than any other mixture tested. The data indicate that the acetates are probably not used as pheromone components.Lepidoptera:Tortricidae:Tortricinae.This research was supported in part by the Rockefeller Foundation and by NSF Grant No. GB-38020.     

Sex pheromone of the avocado pest,Amorbia cuneana (Walsingham) (Lepidoptera: Tortricidae)

The major volatile components in the extract of the female sex pheromone gland ofAmorbia cuneana consisted of (E,E)- and (E,Z)-10,12-tetradecadien-1-ol acetates. The identification was based on electroantennogram bioassay of gas Chromatographic effluent from sex pheromone gland extract, relative retention times on polar and nonpolar gas chromatographic columns, chemical degradation (ozonolysis, saponification), mass spectrometry, chemical synthetic methods, and field tests. Based on mass spectrometry and retention times by capillary gas chromatography, traces of (E)-10-tetradecen-1-ol acetate and 1-tetradecanol acetate were also present in the extract. Traps baited with a combination of synthetic (E,E)- and (E,Z)-10,12-tetradecadien-1-ol acetates caught more males than did traps baited with females.This paper reports the results of research only. Mention of a commercial product in this paper does not constitute a recommendation by the U.S. Department of Agriculture.     

Leaf Volatiles from Nonhost Deciduous Trees: Variation by Tree Species, Season and Temperature, and Electrophysiological Activity in Ips typographus

The leaf volatiles emitted from four nonhost tree species of Ips typographus, i.e. Betula pendula, B. pubescens, Populus tremula, and Sambucus nigra, were collected outdoors by headspace sampling in situ and analyzed by GC-MS. Three major classes of compounds, aliphatics [mainly green-leaf volatiles (GLVs)], monoterpenes, and sesquiterpenes, existed in all the deciduous tree species investigated. In June, when the bark beetles are searching in flight for host trees, GLVs mainly consisting of (Z)-3-hexenyl acetate and (Z)-3-hexen-1-ol were the dominant constituents in B. pendula and S. nigra. In B. pubescens and P. tremula, sesquiterpenes (and their derivatives) and monoterpenes made up the major part of whole volatile blends, respectively. Surprisingly, sesquiterpene alcohols and other oxides released from B. pubescens in considerable amounts were not found in the closely related species, B. pendula. By August, both the total volatiles and individual compounds significantly decreased, mainly due to the maturation of leaves, since the light intensity and temperatures during sampling were the same as in June. There were almost no volatiles detected from P. tremula and S. nigra leaves in August. The total emissions from these deciduous species were significantly different among the species, with B. pubescens releasing 5–10 times more than other species. Under the conditions of constant light intensity and humidity, emissions of both total volatiles and most individual components of severed B. pendula and S. nigra branches (with fresh leaves) increased according to a saturation curve from 16°C to 40°C. Ips typographus antennae responded strongly to green leaf alcohols: (Z)-3-hexen-1-ol, 1-hexanol, and (E)-2-hexen-1-ol, but not to aldehydes or acetates in GC-EAD analyses of B. pendula and B. pubescens leaf volatiles. No antennal responses to monoterpenes, sesquiterpenes, or sesquiterpene oxides were found. These three antennally active GLVs emitted from nonhost tree leaves might be indicators of a wrong habitat in the host selection of conifer bark beetles.     

A Novel Approach for Isolation of Volatile Chemicals Released by Individual Leaves of a Plant in situ

A glass chamber designed specifically for collecting volatile chemicals from individual leaves of a plant in situ is described. The effectiveness of the chamber was demonstrated by collecting volatile chemicals from single leaves of two plant species, potato (Solanum tuberosum) and broad bean (Vicia faba), before and after mechanical damage. The glass chamber, in conjunction with thermal desorption, enables reduction of the entrainment time and thereby allows the monitoring of compounds released by leaf damage in successive 5-min periods. An intact broad bean leaf, in the middle of the day, produces small amounts of the green leaf volatiles (E)-2-hexenal and (Z)-3-hexen-1-ol. However, during the first 5 min after mechanical damage, large amounts of (Z)-3-hexenal, (E)-2-hexenal, and (Z)-3-hexen-1-ol are produced. The decline in production of (Z)-3-hexenal and (E)-2-hexenal is fast, and after 10 min, these compounds reach very low levels. (Z)-3-Hexen-1-ol shows an increase for the first 10 min and then a gradual decline. An intact potato leaf, in the middle of the day, produces very small amounts of the sesquiterpene hydrocarbons -caryophyllene and germacrene-D. After being damaged, the profile of released volatiles is different from that of broad bean. In potato, damage is associated with release of large amounts of green leaf volatiles and sesquiterpene hydrocarbons. Compounds such as (Z)-3-hexenal, (E)-2-hexenal, and (Z)-3-hexen-1-ol are released in high amounts during the first 5 min after damage, but after 10 min, these drop to very low levels. High release associated with damage is also observed for -caryophyllene, (E)--farnesene, germacrene-D, and -bisabolene. The highest level is reached 5 min after damage and 15 min later, these compounds drop to low levels. The significance of compounds released after plant damage is discussed.