Green leaf volatiles enhance aggregation pheromone of boll weevil, Anthonomus grandis

Enhancement of an insect pheromone response by green leaf volatiles is reported for the first time in the boll weevil, Anthonomus grandis Boh. (Coleoptera: Curculionidae). Single cell recordings from antennal olfactory receptors revealed a class of cells selectively responsive to six carbon alcohols and aldehydes (i.e., green leaf volatiles). Field tests with released weevils demonstrated enhanced trap captures with trans-2-hexen-l-ol, cis-3-hexen-l-ol, or l-hexanol paired with grandlure, the boll weevil aggregation pheromone, when in competition with grandlure alone. Although dose-response curves constructed from electroantennograms were indicative of similar populations of receptor cells for selected six carbon alcohols, one of the compounds tested, cis-2-hexen-l-ol, was inactive in field tests. Trans-2-hexenal was active in single cell recordings, but was also inactive in field tests. In tests in cotton fields with indigenous weevil populations, trans-2-hexen-l-ol not only enhanced pheromone trap captures, but also extended the longevity of attractiveness of pheromone-baited traps. The combined electrophysiological and field data support across-fiber coding of green leaf volatiles by boll weevil olfactory receptors. The results are discussed with regard to the chemistry of the host plant of the boll weevil, cotton (Gossypium hirsutum L.), and potential economic significance for boll weevil eradication/suppression.

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Résumé Pour la première fois, l'augmentation de la puissance de la phéromone d'agrégation sous l'action de l'odeur verte est signalée chez A. grandis. Les enregistrements unitaires de cellules des récepteurs olfactifs des antennes a mis en évidence une catégorie de cellules réagissant sélectivement aux alcools et aux aldéhydes à 6 carbones (c'est-à-dire aux substances volatiles des feuilles vertes). Des essais dans la nature ont montré une augmentation des captures par les pièges de grandlure (phéromone d'agrégation du charançon) renforcés par du trans-2-hexen-l-ol, du cis-3-hexen-l-ol, ou du l-hexanol.Bien que les courbes des réponses en fonction des doses construites à partir des électroantennogrammes indiquent des catégories de cellules réceptrices identiques pour les alcools à 6 carbones examinés, l'une de ces substances, cis-2-hexen-l-ol, s'est révélée inactive dans la nature. Le trans-2-hexenal qui était actif avec des enregistrements unitaires de cellules, était lui aussi inactif dans la nature. Dans des essais dans des champs de coton avec des populations indigènes de charançons, le trans-2-hexen-l-ol a, non seulement augmenté l'efficacité des pièges à phéromone, mais a prolongé leur attractivité. Les résultats d'électrophysiologie combinés aux données de la nature appuient le modelage transversal des substances vertes volatiles des feuilles par les récepteurs olfactifs du charançon. Ces résultats sont interprétés en relation avec la chimie de la plante-hôte de A. grandis, le coton, Gossypium hirsutum L., et leur possibilité d'utilisation économique pour l'éradication du charançon.

     

Volatile constituents of the boll weevil

When the distillable oil from adult boll weevils, Anthonomus grandis, of both sexes was investigated with an integrated gas chromatographymass spectrometry system, evidence was obtained for a number of mono- and sesquiterpene hydrocarbons and some substituted anilines including o-toluidine; for some C₅ and C₆ alcohols and monoterpene alcohols; and for at least one sesquiterpene alcohol. The major components were a series of alkanes, alkenes, and alkyl alcohols of high molecular weight. This investigation was part of a study made to identify possible additional components of the pheromone produced by the boll weevil.     

Comparisons of standard and extended-life boll weevil (Coleoptera: Curculionidae) pheromone lures

The Southeastern Boll Weevil Eradication Program has proposed reducing maintenance program costs in eradicated zones by using an extended-life "superlure" in traps to detect populations of the boll weevil, Anthonomus grandis grandis Boheman. However, superlure effectiveness has not been extensively evaluated. We compared the superlure (30 mg of eugenol plus 25 mg of grandlure) to a standard lure (10 mg of grandlure) based on captures of weevils and changes in lure pheromone content. Lure treatments (standard and superlure, replaced biweekly or not replaced) were compared in 4-mo-long trapping periods. Captures of weevils did not generally reflect differences among lure treatments indicated by assays of lure contents. During the first 2 wk of exposure, amounts of pheromone released by the superlure were generally comparable with those of the standard lure, but pheromone composition was more stable. During the second 2 wk of exposure, the superlure usually released more pheromone than similarly aged standard lures, but less than half as much as the standard lure replaced biweekly. Based on numbers of captured weevils during the last 2 wk of an extended trapping period, the superlure performed similarly to the standard lure replaced biweekly. However, corresponding pheromone releases by the superlure were less than those by the standard lure replaced biweekly. This inconsistency suggests that numbers of captured weevils alone may be inadequate for evaluation of pheromone formulations. Our results suggest that better understanding of the consequences of reduced pheromone release during an extended trapping period is needed before adoption of the superlure can be recommended.     

Metabolism of sugars to polyols in the boll weevil

When fed to starved adults of Anthonomus grandis, several pentoses and hexoses were metabolized to the corresponding polyols (sugar alcohols). Xylitol, galactitol, arabitol, ribitol, rhamnitol, mannitol, and sorbitol were metabolites of d-xylose, d-galactose and lactose, d-arabinose, d-ribose, l-rhamnose, d-mannose, and d-glucose and d-fructose, respectively. l-Sorbose was not metabolized to a polyol. Large quantities of xylitol and galactitol and intermediate amounts of arabitol, ribitol, and rhamnitol accumulated while only small amounts or traces of mannitol and sorbitol were detected. The limited accumulation of sorbitol in the glucose- and fructose-fed weevils probably was caused by the rapid metabolism of sorbitol to glucose, fructose, trehalose, and glycogen. Each of the ingested sugars, the corresponding polyols, and trehalose were present in the weevil haemolymph. Most of the polyols had never before been detected as metabolites in an insect.     

Karyotypic analysis of the cotton boll weevil, Anthonomus grandis Boheman

The diploid chromosome number of the cotton boll weevil, Anthonomus grandis Boheman, is 44. Both C‐ and N‐banding techniques of mitotic cells demonstrated constitutive heterochromatin in the p arm of the eight largest chromosomes, the p arm of the X chromosome, and the centromeric region of autosomal groups A–D. Neither the y nor the group E autosomes appeared to contain constitutive heterochromatin. Supernumerary chromosomes were not found in the boll weevil. Restriction endonuclease banding of primary spermatocytes revealed a rod‐shaped Xy tetrad in which the X and y were terminally associated. The p arm of the large, submetacentric X was C‐band positive. While two of the autosomal tetrads were typically ring‐shaped in primary spermatocytes, the remaining 19 autosomal tetrads were rod‐shaped. This revised version was published online in July 2006 with corrections to the Cover Date.     

Evaluation of kill strips on boll weevil (Coleoptera: Curculionidae) mortality in pheromone traps and impact on weevil escape

A field study examined the temporal patterns of boll weevil mortality provided by two commercially available kill strips, Hercon VaporTape II and Plato Insecticide Strip, and to evaluate the impacts of these devices on weevil escape from traps. Both types of kill strips produced similar levels of weevil mortality with the exception of the last two inspection intervals (30 and 46 h after continual exposure to kill strips). At these intervals, the Plato Strip produced significantly higher mortality than the Hercon strip; however, these differences were numerically small (10 and 6%, respectively). Both types of kill strips produced a high level of weevil mortality in traps (> 90%) after 46 h of exposure. On average, 5-8% of weevils escaped from traps whether a kill strip was present or absent. A strong temporal pattern of escape was observed, with > or = 90% of escape occurring within the first hour after weevils were introduced into traps. Because > or = 90% of escape occurred within the first hour weevils were in the traps and < 3% of weevils died during the first hour of exposure to kill strips in traps, use of kill strips in large-scale boll weevil management programs is not justified on the basis of reduced weevil escape.     

Site of pheromone biosynthesis and isolation of HMG-CoA reductase cDNA in the cotton boll weevil, Anthonomus grandis

Isolated gut tissue from male cotton boll weevil, Anthonomus grandis (Coleoptera: Curculionidae), incorporated radiolabeled acetate into components that co-eluted with monoterpenoid pheromone components on HPLC. This demonstrates that pheromone components of male A. grandis are produced de novo and strongly suggests that pheromone biosynthesis occurs in gut tissue. A central enzyme in isoprenoid biosynthesis is 3-hydroxy-3-methylglutaryl-CoA reductase (HMG-R), and a full-length HMG-R cDNA was isolated from A. grandis. The predicted translation product was 54 and 45% identical to HMG-R from Ips paraconfusus and Drosophila melanogaster, respectively. HMG-R gene expression gradually increased with age in male A. grandis, which correlates with pheromone production. However, topical application of JH III did not significantly increase HMG-R mRNA levels.     

Fine-tuning the composition of the cranberry weevil (Coleoptera: Curculionidae) aggregation pheromone

The cranberry weevil Anthonomus musculus Say is a key pest of highbush blueberries (Vaccinium corymbosum L.) and cranberries (Vaccinium macrocarpon Aiton) in the northeastern United States. Previous studies have reported A. musculus adult attraction to traps baited with the aggregation pheromone of the pepper weevil Anthonomus eugenii Cano, likely because these two weevils share similar pheromone blends that differ only in two components. The A. musculus aggregation pheromone contains (Z)-2-(3,3-dimethylcyclohexylidene) ethanol (Z grandlure II), (Z)-(3,3-dimethylcyclohexylidene) acetaldehyde (grandlure III), (E)-(3,3-dimethylcyclohexylidene) acetaldehyde (grandlure IV) and (E)-3,7-dimethyl-2,6-octadien-1-ol (geraniol); whereas A. eugenii produces a pheromone blend that includes (E)-2-(3,3-dimethylcyclohexylidene) ethanol (E grandlure II) and (E)-3,7-dimethyl-2,6-octadienoic acid (geranic acid) in addition to the four A. musculus pheromone components. Here, we hypothesized that differences in pheromone composition between these two species influence A. musculus adult attraction to its aggregation pheromone. To test this, we studied the response of A. musculus to its pheromone blend with and without E grandlure II and geranic acid, a commercial A. eugenii pheromone lure and a no-lure control in highbush blueberry and cranberry fields in New Jersey and Massachusetts, respectively. Regardless of crop type, A. musculus adults were more attracted to their four-component pheromone blend and the blend plus geranic acid than the commercial A. eugenii pheromone and the no-lure controls. The A. musculus pheromone blend plus E grandlure II and the A. eugenii pheromone blend also captured more A. musculus adults than the no-lure control but not compared to the commercial A. eugenii pheromone. Further analysis showed that A. musculus adults are significantly (~27%) less attracted to their pheromone blend if it contains E grandlure II, although the addition of geranic acid did not affect their response. These findings may help guide future efforts towards the development of behaviour-based tools to monitor and manage A. musculus.     

Susceptibility of the boll weevil to Steinernema riobrave and other entomopathogenic nematodes

The susceptibility of the boll weevil (BW), Anthonomus grandis Boheman, to Steinernema riobrave and other nematode species in petri dishes, soil (Hidalgo sandy clay loam), and cotton bolls and squares was investigated. Third instar weevils were susceptible to entomopathogenic nematode (EN) species and strains in petri dish bioassays at 30 degrees C. Lower LC(50)'s occurred with S. riobrave TX- 355 (2 nematodes per weevil), S. glaseri NC (3), Heterorhabditis indicus HOM-1 (5), and H. bacteriophora HbL (7) than H. bacteriophora IN (13), S. riobrave TX (14), and H. bacteriophora HP88 (21). When infective juveniles (IJs) of S. riobrave were applied to weevils on filter paper at 25 degrees C, the LC(50) of S. riobrave TX for first, second, and third instars, pupae, and 1-day-old and 10-days-old adult weevils were 4, 5, 4, 12, 13, and 11IJs per weevil, respectively. The mean time to death, from lowest to highest concentration, for the first instar (2.07 and 1.27days) and second instar (2.55 and 1.39days) weevils were faster than older weevil stages. But, at concentrations of 50 and 100IJs/weevil, the mean time to death for the third instar, pupa and adult weevils were similar (1.84 and 2.67days). One hundred percent weevil mortality (all weevil stages) occurred 3days after exposure to 100IJs per weevil. Invasion efficiency rankings for nematode concentration were inconsistent and changed with weevil stage from 15 to 100% when weevils were exposed to 100 and 1IJs/weevil, respectively. However, there was a consistent relationship between male:female nematode sex ratio (1:1.6) and nematode concentration in all infected weevil stages. Nematode production per weevil cadaver increased with increased nematode concentrations. The overall mean yield of nematodes per weevil was 7680IJs. In potted soil experiments (30 degrees C), nematode concentration and soil moisture greatly influenced the nematode efficacy. At the most effective concentrations of 200,000 and 400,000IJs/m(2) in buried bolls or squares, higher insect mortalities resulted in pots with 20% soil moisture either in bolls (94 and 97% parasitism) or squares (92 and 100% parasitism) than those of 10% soil moisture in bolls (44 and 58% parasitism) or squares (0 and 13% parasitism). Similar results were obtained when nematodes were sprayed on the bolls and squares on the soil surface. This paper presents the first data on the efficacy of S. riobrave against the boll weevil, establishes the potential of EN to control the BW inside abscised squares and bolls that lay on the ground or buried in the soil.     

Biosynthesis of grandlure,the pheromone of the boll weevil,Anthonomus grandis,from acetate,mevalonate, and glucose

The steam-distilled faeces of adult male boll weevils, Anthonomus grandis, that had been injected with acetate-1¹⁴C, acetate-2¹⁴C, mevalonic acid-2¹⁴C, or glucose¹⁴C(U) showed by column and gas chromatography that approximately 0·02 per cent of the administered radioactivity was incorporated into the volatile fraction. Also, 4 components of the pheromone comprised 57 to 80 per cent of the radioactivity of the volatiles but only 39 per cent of the total content of volatiles. Thus, evidence was obtained for de novo synthesis of the components. Although the boll weevil is essentially an obligate insect of cotton, this insect does not appear to require any specific component in cotton for biosynthesis of the pheromone.     

Forensic pollen geolocation techniques used to identify the origin of boll weevil re-infestation

The boll weevil, Anthonomus grandis, entered the United States of America in the early twentieth century and became a major pest in cotton, Gossypium spp. Shortly after the passage of Tropical Storm Erin on 16 August 2007 through the South Texas/Winter Garden boll weevil eradication zone, over 150 boll weevils were captured in the Southern Rolling Plains (SRP) eradication zone that was essentially weevil-free since 2003. Pollen analyses were made of the SRP weevils and weevils collected in two suspected source zones, Cameron (Southern Blacklands eradication zone) and Uvalde (Winter Garden eradication zone). An additional examination of the palynological evidence and examination of additional pollen residue shed new light on this event and strengthens the conclusion that the Uvalde area was the source of the SRP weevils. A total of 192 pollen grains from 39 taxa were found in the SRP weevils: 1904 pollen grains from ten taxa from the Cameron weevils and 148 grains from 28 taxa in the Uvalde weevils. The SRP weevils shared 16 taxa, including Phermeranthus sp. (flameflower) with the Uvalde weevils and only five taxa with the Cameron weevils. Common taxa between SRP and Uvalde weevils and the lack of the dominant ‘low spine’ Asteraceae that occurred in all Cameron samples confirm that the SRP weevils originated from the South Texas/Winter Garden zone. Problems associated with this type of research are similar to those in forensic palynology. These problems include the unknown origin of the weevils, pollen contamination and care and storage of the samples.     

Evaluation of extended-life pheromone formulations used with and without dichlorvos for boll weevil (Coleoptera: Curculionidae) trapping

Boll weevil traps baited with a ComboLure (25 of mg grandlure + 30 mg of eugenol + 90 of mg dichlorvos [DDVP]), an extended-release lure (25 mg of grandlure + 30 mg of eugenol + 60 of mg DDVP kill-strip), and extended-release lure with no DDVP were evaluated for boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), captures in South Texas cotton, Gossypium hirsutum L., fields during February-March 2005 and March-April 2006. The traps were serviced once a week for five consecutive weeks by using the same methodology as active boll weevil eradication programs. Mean captured boll weevils from extended-release lures with no DDVP were significantly higher in five of 10 trapping weeks compared with captures of the ComboLure and extended lure. Weekly mortality of boll weevils captured was similar for the ComboLure (72.6 +/- 4.7%) and extended lure + DDVP (73.5 +/- 4.0%), and both were significantly higher than the extended lure (32.8 +/- 5.0%) with no DDVP. The presence or absence of DDVP did not significantly affect the sex ratio of field-captured boll weevils. We found no functional reasoning for using DDVP in large scale trapping of boll weevils regardless of the formulation or presentation in the trap. We conducted two additional trapping evaluations after the 2005 and 2006 studies, but the numbers of boll weevils captured were too low for statistical comparisons, indicating that boll weevil eradication is reducing populations in the Rio Grande Valley of Texas.     

The use of aggregation pheromone to enhance dissemination of Beauveria bassiana for the control of the banana weevil in Uganda

Candidate strains of Beauveria bassiana were identified for use in integrated pest management of the banana weevil Cosmopolites sordidus. Horizontal field transmission of B. bassiana between banana weevils using different delivery systems, including aggregation pheromones, was investigated. We observed that infected weevils could transmit the fungal pathogen to healthy individuals. Most dead weevils (52%) due to B. bassiana infection were found at the base of banana plants in the leaf sheath or in the soil near banana plants. Significantly more weevils died from the pathogen in plots where B. bassiana was applied in combination with the pheromone than where it was applied alone. Our data demonstrate that C. sordidus aggregation pheromone can be a valuable tool to enhance the dissemination of B. bassiana for the control of C. sordidus.     

A host monoterpene influences Ips typographus (Coleoptera: Curculionidae,Scolytinae) responses to its aggregation pheromone

1 Host tree terpenes can influence attraction of conifer‐infesting bark beetles to their aggregation pheromones, and both synergistic and inhibitory effects have been reported. 2 We tested a gradient of ratios of (–)‐α‐pinene, the predominant monoterpene in Norway spruce, to the pheromone of Ips typographus, a major pest of Norway spruce. 3 Attraction of I. typographus increased as the release rate of (–)‐α‐pinene increased. The two highest (–)‐α‐pinene : pheromone ratios (526 : 1 and 2595 : 1) attracted twice as many I. typographus as pheromone alone, whereas low to intermediate ratios (56 : 1, 274 : 1) did not differ from pheromone alone. 4 Our results are in agreement with a proposed model, which suggests that bark beetles display unique response profiles to host terpenes depending on the physiological condition of the host trees that they typically colonize. Ips typographus, which is an aggressive species capable of colonizing and killing healthy trees, showed an increased attraction to monoterpene : pheromone ratios, and this may be high enough to inhibit attraction of less aggressive beetle species typically colonizing dead, dying or stressed trees. 5 Attraction of associates of I. typographus was also modified by (–)‐α‐pinene. Ips duplicatus, a competitor of I. typographus, showed increased attraction to the pheromone of I. typographus across all concentrations of (–)‐α‐pinene.     

Host odours enhance the responses of adult Rhyzopertha dominica to male-produced aggregation pheromone

The behavioural responses of adult male and female Rhyzopertha dominica (Coleoptera, Bostrichidae) to blends of host volatiles and male-produced aggregation pheromone were observed in a four-arm airflow olfactometer. The odour sources used were five pheromone-releasing males each on a single maize grain (lower maize-volatiles blend), five pheromone-releasing males on 500 g of maize (higher maize-volatiles blend) or the host volatiles emanating from 500g of maize (maize volatiles alone). Multiple-choice tests, in which volatiles from all three odour sources were presented in the exposure chamber at the same time, were used to study odour preferences of the males and females. Both sexes showed strongest attraction to the higher maize volatile blend but there were significant sex differences in response to the odour sources. Males spent significantly more time than females in the zone with only maize volatiles, and females spent significantly more time in the higher maize-volatiles zone. However, when odour sources were offered singly, females gave numerically greater responses than males to all sources although this difference was statistically significant for only the lower maize-volatiles blend. As males are more attracted than females to host odours alone it is suggested that they may be more highly adapted to seek out new hosts while females are more inclined to locate a food source by following the pheromone signals produced by males. However, both sexes responded most strongly to the odour source comprising aggregation pheromone with the higher proportion of maize volatiles.     

Infection of the boll weevil by Chilo iridescent virus

When infections with Chilo iridescent virus (CIV) were induced in larvae of boll weevils, Anthonomus grandis, by intrahemocoelic injection or by feeding, and in adults by feeding, the typical blue coloration of adipose tissue developed at 3–7 days postinfection, and mortality occurred after 3 days. The symptomatology and the pathological expressions depended on the initial infectious titer. The virus remained viable when it was added to the feeding stimulant bait used to infect weevils with protozoan pathogens in the field, and weevils feeding on the formulation became infected when it had been exposed 1–3 days in nature.     

Factors influencing response of flying Prostephanus truncatus to its male-produced aggregation pheromone

Abstract. The effects of age, sex, mating status, pre-exposure to pheromone, resource (diet) quality, and starvation on the response of Prostephanus truncatus (Horn) (Coleoptera: Bostrichidae) to its male-produced aggregation pheromone were investigated.Age was an important factor determining the level of response to pheromone: young adults were more responsive than older adults.The suitability of the resource in which P.truncatus is present affected its dispersal tendency, but not its sensitivity to pheromone per se. Sex, mating status, brief prior exposure to pheromone, and starvation did not influence the response of the larger grain borer to pheromone.The orientation behaviour of the beetle is described, and it is proposed that the pheromone primarily functions as a 'suitable resource location and colonization signal'.