Ann M. Ray
Xavier University
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Featured researches published by Ann M. Ray.
Journal of Chemical Ecology | 2007
Lawrence M. Hanks; Jocelyn G. Millar; Jardel A. Moreira; James D. Barbour; Emerson S. Lacey; J. Steven McElfresh; F. Ray Reuter; Ann M. Ray
Males of several species of longhorned beetles in the subfamily Cerambycinae produce sex or aggregation pheromones consisting of 2,3-hexanediols and/or hydroxyhexanones. We tested the hypothesis that this diol/hydroxyketone pheromone motif is highly conserved within the subfamily, and the resulting prediction that multiple cerambycine species will be attracted to compounds of this type. We also tested the concept that live traps baited with generic blends of these compounds could be used as a source of live insects from which pheromones could be collected and identified. Traps placed in a mature oak woodland and baited with generic blends of racemic 2-hydroxyhexan-3-one and 3-hydroxyhexan-2-one captured adults of both sexes of three cerambycine species: Xylotrechus nauticus (Mannerheim), Phymatodes lecontei Linsley, and Phymatodes decussatus decussatus (LeConte). Odors collected from male X. nauticus contained a 9:1 ratio of two male-specific compounds, (R)- and (S)-3-hydroxyhexan-2-one. Field trials with synthetic compounds determined that traps baited with (R)-3-hydroxyhexan-2-one (94% ee), alone or in blends with other isomers, attracted similar numbers of X. nauticus of both sexes, whereas (S)-3-hydroxyhexan-2-one (94% ee) attracted significantly fewer beetles. Phymatodes lecontei and P. d. decussatus also were caught in traps baited with hydroxyhexanones, as well as a few specimens of two other cerambycine species, Neoclytus modestus modestus Fall (both sexes) and Brothylus gemmulatus LeConte (only females). Male N. m. modestus produced (R)-3-hydroxyhexan-2-one, which was not present in extracts from females. Neoclytus m. modestus of both sexes also responded to lures that included (R)-3-hydroxyhexan-2-one as one of the components. The only male-specific compound found in extracts from P. lecontei was (R)-2-methylbutan-1-ol, and adults of both sexes were attracted to racemic 2-methylbutan-1-ol in field bioassays. Surprisingly, P. lecontei of both sexes also were attracted to (R)- and (S)-3-hydroxyhexan-2-ones, although neither compound was detected in extracts from this species. Males of all five beetle species had gland pores on their prothoraces that were similar in structure to those that have been associated with volatile pheromone production in other cerambycine species. The attraction of multiple cerambycine species of two tribes to (R)-3-hydroxyhexan-2-one in this study, and in earlier studies with other cerambycine species, suggests that this compound is a widespread aggregation pheromone component in this large and diverse subfamily. Overall, the attraction of multiple species from different cerambycine tribes to this compound at a single field site supports the hypothesis that the hydroxyketone pheromone structural motif is highly conserved within this subfamily.
Entomologia Experimentalis Et Applicata | 2007
Emerson S. Lacey; Jardel A. Moreira; Jocelyn G. Millar; Ann M. Ray; Lawrence M. Hanks
Adult male Neoclytus mucronatus mucronatus (F.) (Coleoptera: Cerambycidae: Cerambycinae) were observed to display behaviors identical to calling behaviors of the congener N. acuminatus acuminatus F., males of which produce an aggregation pheromone. Odors collected from male N. m. mucronatus contained one major male‐specific compound, identified as (R)‐3‐hydroxyhexan‐2‐one. Bioassays determined that both sexes were weakly attracted to racemic 3‐hydroxy‐2‐hexanone. Further field trials determined that enantiomerically enriched (R)‐3‐hydroxyhexan‐2‐one (94% ee) attracted more beetles of both sexes than did the racemic blend. This aggregation pheromone is produced by glands that discharge through pores lying within shallow cuticular depressions in the pronotum of male N. m. mucronatus.
Journal of Chemical Ecology | 2009
Ann M. Ray; Jocelyn G. Millar; J. Steven McElfresh; Ian P. Swift; James D. Barbour; Lawrence M. Hanks
We report the identification, synthesis, and field bioassays of a volatile, male-produced aggregation pheromone of a long-horned beetle, the banded alder borer, Rosalia funebris Mots. Headspace collections from males contained a major male-specific compound, (Z)-3-decenyl (E)-2-hexenoate, and several minor components, identified as (Z)-3-decenol, (Z)-3-nonenyl (E)-2-hexenoate, and (Z)-3-decenyl (E)-3-hexenoate. The antennae of both males and females responded strongly to (Z)-3-decenyl (E)-2-hexenoate. We collected significant numbers of adult R. funebris in field bioassays using traps baited with this compound. This pheromone structure is unprecedented in the literature of cerambycid pheromones and distinct from the more common diol/hydroxyketone pheromone motif of many other species of the diverse subfamily Cerambycinae. This is the first pheromone identified for a species in the tribe Rosaliini.
Naturwissenschaften | 2006
Ann M. Ray; Emerson S. Lacey; Lawrence M. Hanks
Males of five species of three tribes in the longhorned beetle subfamily Cerambycinae produce volatile pheromones that share a structural motif (hydroxyl or carbonyl groups at carbons two and three in straight-chains of six, eight, or ten carbons). Pheromone gland pores are present on the prothoraces of males, but are absent in females, suggesting that male-specific gland pores could provide a convenient morphological indication that a species uses volatile pheromones. In this article, we assess the taxonomic distribution of gland pores within the Cerambycinae by examining males and females of 65 species in 24 tribes using scanning electron microscopy. Gland pores were present in males and absent in females of 49 species, but absent in both sexes of the remaining 16 species. Pores were confined to indentations in the cuticle. Among the species that had male-specific gland pores were four species already known to produce volatile compounds consistent with the structural motif. These findings support the initial assumption that gland pores are associated with the production of pheromones by males. There were apparently no taxonomic patterns in the presence of gland pores. These findings suggest that volatile pheromones play an important role in reproduction for many species of the Cerambycinae, and that the trait is evolutionarily labile.
Journal of Chemical Ecology | 2006
Matthew D. Ginzel; Jardel A. Moreira; Ann M. Ray; Jocelyn G. Millar; Lawrence M. Hanks
Male Megacyllene caryae (Gahan) (Coleoptera: Cerambycidae) respond to females only after touching them with their antennae, indicating that mate recognition is mediated by a contact sex pheromone. Gas chromatography-mass spectrometry analyses of whole-body solvent extracts of male and female M. caryae revealed substantial differences in hydrocarbon profiles, with nearly half of the compounds in the extracts from females being absent from those of males. Biological activities of fractions of crude extracts of females, and reconstructed blends of the most abundant straight-chain (nC27, nC28, nC29), methyl-branched (2Me-C26, 9Me-C29, 11, 13, 15Me-C29), and unsaturated (Z9:C29, Z13:C29, Z14:C29, Z13:C31, Z14:C31, Z15:C31) compounds in extracts of females were tested in arena bioassays, assessing four steps in the mating behavior sequence of males (orientation, arrestment, body alignment, mounting and attempting to couple the genitalia). Males showed limited response to dead females treated with fractions of the crude extract or blends of synthetic straight-chain and methyl-branched alkanes, but responded strongly to the blend of synthetic monoenes. Further trials determined that the complete sequence of mating behaviors, up to and including coupling the genitalia, was elicited by Z9:C29 alone. Z9:C29 is a homolog of the contact pheromone (Z9:C25) of the congener M. robiniae (Förster). Previous work with M. robiniae suggested that wipe sampling of cuticular hydrocarbons of females by solid phase microextraction yielded a more representative profile of components actually encountered by a male’s antennae, and so provided a more readily interpretable profile of potential semiochemicals present in the wax layer than does solvent extraction. We tested this hypothesis by comparing hydrocarbon profiles of female M. caryae by the two sampling methods. Z9:C29 was the only compound among the dominant hydrocarbons that was present in higher abundance in SPME than in solvent extracts (∼12% vs. ∼8%, respectively), supporting this hypothesis.
Genome Biology | 2016
Duane D. McKenna; Erin D. Scully; Yannick Pauchet; Kelli Hoover; Roy Kirsch; Scott M. Geib; Robert F. Mitchell; Robert M. Waterhouse; Seung Joon Ahn; Deanna Arsala; Joshua B. Benoit; Heath Blackmon; Tiffany Bledsoe; Julia H. Bowsher; André Busch; Bernarda Calla; Hsu Chao; Anna K. Childers; Christopher Childers; Dave J. Clarke; Lorna Cohen; Jeffery P. Demuth; Huyen Dinh; HarshaVardhan Doddapaneni; Amanda Dolan; Jian J. Duan; Shannon Dugan; Markus Friedrich; Karl M. Glastad; Michael A. D. Goodisman
BackgroundRelatively little is known about the genomic basis and evolution of wood-feeding in beetles. We undertook genome sequencing and annotation, gene expression assays, studies of plant cell wall degrading enzymes, and other functional and comparative studies of the Asian longhorned beetle, Anoplophora glabripennis, a globally significant invasive species capable of inflicting severe feeding damage on many important tree species. Complementary studies of genes encoding enzymes involved in digestion of woody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 additional insects, including the newly sequenced emerald ash borer and bull-headed dung beetle.ResultsThe Asian longhorned beetle genome encodes a uniquely diverse arsenal of enzymes that can degrade the main polysaccharide networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woody plants. It has the metabolic plasticity needed to feed on diverse plant species, contributing to its highly invasive nature. Large expansions of chemosensory genes involved in the reception of pheromones and plant kairomones are consistent with the complexity of chemical cues it uses to find host plants and mates.ConclusionsAmplification and functional divergence of genes associated with specialized feeding on plants, including genes originally obtained via horizontal gene transfer from fungi and bacteria, contributed to the addition, expansion, and enhancement of the metabolic repertoire of the Asian longhorned beetle, certain other phytophagous beetles, and to a lesser degree, other phytophagous insects. Our results thus begin to establish a genomic basis for the evolutionary success of beetles on plants.
Journal of Chemical Ecology | 2009
Joshua Rodstein; J. Steven McElfresh; James D. Barbour; Ann M. Ray; Lawrence M. Hanks; Jocelyn G. Millar
Females of the large cerambycid beetle Prionus californicus produce a powerful sex pheromone that attracts males. The pheromone was adsorbed on solid phase microextraction (SPME) fibers inserted into the ovipositor sheath and analyzed by coupled gas chromatography-electroantennogram detection and GC-mass spectrometry. The pheromone was identified as an isomer of 3,5-dimethyldodecanoic acid by a combination of retention index comparisons and mass spectral interpretation. The mass spectrum was misleading because it exhibited enlarged fragment ions that were not representative of branch points or other obvious stabilizing structural elements. The structure was verified by synthesis of 3,5-dimethyldodecanoic acid as a mixture of all four possible isomers, and this mixture was highly attractive to male beetles in field bioassays. The SPME extracts also contained several other compounds that were tentatively identified as chain-extended homologs of the main pheromone component. This pheromone should prove useful for sampling and management of the beetle, which is an important pest of hops, and an occasional pest in a variety of orchard crops. Although this is the first female-produced pheromone to be identified from the Cerambycidae, there is considerable evidence for pheromone production by females of other species in the subfamily Prioninae. Thus, this pheromone and the associated methodology used in its identification should be useful in the identification of female-produced attractant pheromones from other members of the subfamily.
Annals of The Entomological Society of America | 2011
James D. Barbour; Jocelyn G. Millar; Joshua Rodstein; Ann M. Ray; Diane Alston; Martin Rejzek; James D. Dutcher; Lawrence M. Hanks
ABSTRACT n Males of the longhorned beetle Prionus californicus Motschulsky (Coleoptera: Cerambycidae) are significantly attracted to the female-produced sex pheromone (3R,5S)-3,5-dimethyldodecanoic acid. Males respond equally well to the synthetic blend of the four stereoisomers of 3,5-dimethyldodecanoic acid as to the single natural enantiomer, suggesting that the unnatural isomers are not inhibitory. Males of the congener Prionus lecontei Lameere also are attracted to the (3R,5S)-enantiomer but not to the (3S,5R)-enantiomer, suggesting that the (3R,5S)-enantiomer is also an important pheromone component of that species. Here, we report the results of field trials that test the hypothesis that synthetic 3,5-dimethyldodecanoic acid will serve as a general attractant for males of other Prionus species. We conducted field bioassays of synthetic 3,5-dimethyldodecanoic acid at study sites in six different regions of North America and one site in the United Kingdom. Traps baited with the synthetic pheromone blend captured males of P. californicus (southwestern Idaho, southern California, and northwestern Utah), P. lecontei (southern California and northwestern Utah), and six additional species of Prionus: Prionus integer LeConte (southwestern Idaho), Prionus imbricornis (L.) (Georgia), Prionus laticollis (Drury) (Georgia), Prionus linsleyi Hovore (north central Arizona), Prionus aztecus Casey (northern Mexico), and Prionus coriarius (L.) (East Anglia, United Kingdom). These findings demonstrate that synthetic 3,5-dimethyldodecanoic acid can be used to assess the geographic distribution and local abundance of many Prionus species and therefore may be of value for monitoring threatened and endangered species of this genus, and for managing those that are pests.
Journal of Chemical Ecology | 2011
Ann M. Ray; Alenka Žunič; Ronald L. Alten; J. Steven McElfresh; Lawrence M. Hanks; Jocelyn G. Millar
We report the identification, synthesis, and field bioassays of a female-produced sex attractant pheromone component of the cerambycid beetle Ortholeptura valida (LeConte). Headspace volatiles from females contained a female-specific compound, (Z)-11-octadecen-1-yl acetate, which elicited a strong response from antennae of adult males in coupled gas chromatography-electroantennogram analyses. In field bioassays, significant numbers of males were collected by traps baited with this compound. The pheromone represents a new structural class of cerambycid pheromones, and is the first pheromone identified for a cerambycid species in the subfamily Lepturinae.
Journal of Chemical Ecology | 2011
Joshua Rodstein; Jocelyn G. Millar; James D. Barbour; J. Steven McElfresh; Ian M. Wright; Karen S. Barbour; Ann M. Ray; Lawrence M. Hanks
We previously identified the basic structure of the female-produced sex attractant pheromone of the cerambycid beetle, Prionus californicus Motschulsky (Cerambycidae: Prioninae), as 3,5-dimethyldodecanoic acid. A synthesized mixture of the four stereoisomers of 3,5-dimethyldodecanoic acid was highly attractive to male beetles. Here, we describe stereoselective syntheses of three of the four possible stereoisomers, and the results of laboratory and field bioassays showing that male beetles are attracted specifically to (3R,5S)-3,5-dimethyldodecanoic acid, but not to its enantiomer, (3S,5R)-3,5-dimethyldodecanoic acid, indicating that the (3R,5S)-enantiomer is the active pheromone component. The diastereomeric (3R,5R)- and (3S,5S)-enantiomers were excluded from consideration because their gas chromatographic retention times were different from that of the insect-produced compound. The mixture of the four stereoisomers of 3,5-dimethyldodecanoic acid was as attractive to male P. californicus as the (3R,5S)-enantiomer, indicating that none of the other three stereoisomers inhibited responses to the active enantiomer. Beetles responded to as little as 10xa0ng and 10xa0μg of synthetic 3,5-dimethyldodecanoic acid in laboratory and field studies, respectively. Field studies indicated that capture rate did not increase with dosages of 3,5-dimethyldodecanoic acid greater than 100xa0μg. In field bioassays, males of a congeneric species, P. lecontei Lameere, were captured in southern California but not in Idaho.