{"id":61,"date":"2015-09-14T13:14:23","date_gmt":"2015-09-14T13:14:23","guid":{"rendered":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/?p=61"},"modified":"2017-07-25T18:09:04","modified_gmt":"2017-07-25T18:09:04","slug":"references","status":"publish","type":"post","link":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/2015\/09\/14\/references\/","title":{"rendered":"References"},"content":{"rendered":"

The following bibliography highlights research underpinning or related to the project.<\/h4>\n
    \n
  1. Murlis, J., Elkinton, J. S. & Carde, R. T. Odor Plumes and How Insects Use Them. Annu Rev Entomol<\/em> 37<\/strong>, 505-532 (1992).<\/li>\n
  2. Baker, T. C., Fadamiro, H. Y. & Cosse, A. A. Moth uses fine tuning for odour resolution. Nature<\/em> 393<\/strong>, 530-530 (1998).<\/li>\n
  3. Fadamiro, H. Y., Cosse, A. A. & Baker, T. C. Fine-scale resolution of closely spaced pheromone and antagonist filaments by flying male Helicoverpa zea<\/em>. Journal of Comparative Physiology A<\/em> 185<\/strong>, 11 (1999).<\/li>\n
  4. Nikonov, A. A. & Leal, W. S. Peripheral coding of sex pheromone and a behavioral antagonist in the Japanese beetle, Popillia japonica. J Chem Ecol<\/em> 28<\/strong>, 1075-1089 (2002).<\/li>\n
  5. Andersson, M. N., Binyameen, M., Sadek, M. M. & Schlyter, F. Attraction modulated by spacing of pheromone components and anti-attractants in a bark beetle and a moth. J Chem Ecol<\/em> 37<\/strong>, 899-911, doi:10.1007\/s10886-011-9995-3 (2011).<\/li>\n
  6. Szyszka, P., Stierle, J. S., Biergans, S. & Galizia, C. G. The Speed of Smell: Odor-Object Segregation within Milliseconds. PloS one<\/em> 7<\/strong>, e36096 (2012).<\/li>\n
  7. Stierle, J. S., Galizia, C. G. & Szyszka, P. Millisecond stimulus onset-asynchrony enhances information about components in an odor mixture. The Journal of neuroscience : the official journal of the Society for Neuroscience<\/em> 33<\/strong>, 6060-6069, doi:10.1523\/JNEUROSCI.5838-12.2013 (2013).<\/li>\n
  8. Hopfield, J. J. Olfactory Computation and Object Perception. P Natl Acad Sci USA<\/em> 88<\/strong>, 6462-6466 (1991).<\/li>\n
  9. Broome, B. M., Jayaraman, V. & Laurent, G. Encoding and decoding of overlapping odor sequences. Neuron<\/em> 51<\/strong>, 467-482, doi:DOI 10.1016\/j.neuron.2006.07.018 (2006).<\/li>\n
  10. Nowotny, T., Stierle, J. S., Galizia, C. G. & Szyszka, P. Data-driven honeybee antennal lobe model suggests how stimulus-onset asynchrony can aid odour segregation. Brain research<\/em> 1536<\/strong>, 119-134, doi:10.1016\/j.brainres.2013.05.038 (2013).<\/li>\n
  11. Saha, D. et al.<\/em> A spatiotemporal coding mechanism for background-invariant odor recognition. Nature neuroscience<\/em> 16<\/strong>, 1830-1839, doi:10.1038\/nn.3570 (2013).<\/li>\n
  12. Frisch, K. v. Tanzsprache und Orientierung der Bienen. Springer, Heidelberg<\/em> (1965).<\/li>\n
  13. Waser, N. M. Flower Constancy – Definition, Cause, and Measurement. Am Nat<\/em> 127<\/strong>, 593-603, doi:Doi 10.1086\/284507 (1986).<\/li>\n
  14. Menzel, R. The honeybee as a model for understanding the basis of cognition. Nature reviews. Neuroscience<\/em> 13<\/strong>, 758-768, doi:10.1038\/nrn3357 (2012).<\/li>\n
  15. Sandoz, J. C. Behavioral and neurophysiological study of olfactory perception and learning in honeybees. Frontiers in systems neuroscience<\/em> 5<\/strong>, 98, doi:10.3389\/fnsys.2011.00098 (2011).<\/li>\n
  16. Vickers, N. J. Mechanisms of animal navigation in odor plumes. The Biological bulletin<\/em> 198<\/strong>, 203-212 (2000).<\/li>\n
  17. Vosshall, L. B., Wong, A. M. & Axel, R. An olfactory sensory map in the fly brain. Cell<\/em> 102<\/strong>, 147-159 (2000).<\/li>\n
  18. Sachse, S., Rappert, A. & Galizia, C. G. The spatial representation of chemical structures in the antennal lobe of honeybees: steps towards the olfactory code. The European journal of neuroscience<\/em> 11<\/strong>, 3970-3982 (1999).<\/li>\n
  19. Menzel, R. The insect mushroom body, an experience-dependent recoding device. Journal of physiology, Paris<\/em>, doi:10.1016\/j.jphysparis.2014.07.004 (2014).<\/li>\n
  20. Szyszka, P., Ditzen, M., Galkin, A., Galizia, C. G. & Menzel, R. Sparsening and temporal sharpening of olfactory representations in the honeybee mushroom bodies. Journal of neurophysiology<\/em> 94<\/strong>, 3303-3313, doi:10.1152\/jn.00397.2005 (2005).<\/li>\n
  21. Smith, B. H. Analysis of interaction in binary odorant mixtures. Physiology & behavior<\/em> 65<\/strong>, 397-407 (1998).<\/li>\n
  22. Jinks, A. & Laing, D. G. The analysis of odor mixtures by humans: evidence for a configurational process. Physiology & behavior<\/em> 72<\/strong>, 51-63 (2001).<\/li>\n
  23. Riffell, J. A. et al.<\/em> Flower discrimination by pollinators in a dynamic chemical environment. Science<\/em> (2014).<\/li>\n
  24. Joerges, J., Kuttner, A., Galizia, C. G. & Menzel, R. Representations of odours and odour mixtures visualized in the honeybee brain. Nature<\/em> 387<\/strong>, 285-288 (1997).<\/li>\n
  25. Silbering, A. F. & Galizia, C. G. Processing of odor mixtures in the Drosophila antennal lobe reveals both global inhibition and glomerulus-specific interactions. The Journal of neuroscience : the official journal of the Society for Neuroscience<\/em> 27<\/strong>, 11966-11977, doi:10.1523\/JNEUROSCI.3099-07.2007 (2007).<\/li>\n
  26. Deisig, N., Giurfa, M., Lachnit, H. & Sandoz, J. C. Neural representation of olfactory mixtures in the honeybee antennal lobe. The European journal of neuroscience<\/em> 24<\/strong>, 1161-1174, doi:10.1111\/j.1460-9568.2006.04959.x (2006).<\/li>\n
  27. Lei, H. & Vickers, N. Central processing of natural odor mixtures in insects. J Chem Ecol<\/em> 34<\/strong>, 915-927, doi:10.1007\/s10886-008-9487-2 (2008).<\/li>\n
  28. Deisig, N., Giurfa, M. & Sandoz, J. C. Antennal lobe processing increases separability of odor mixture representations in the honeybee. Journal of neurophysiology<\/em> 103<\/strong>, 2185-2194, doi:10.1152\/jn.00342.2009 (2010).<\/li>\n
  29. Faber, T., Joerges, J. & Menzel, R. Associative learning modifies neural representations of odors in the insect brain. Nature neuroscience<\/em> 2<\/strong>, 74-78 (1999).<\/li>\n
  30. Szyszka, P., Galkin, A. & Menzel, R. Associative and non-associative plasticity in kenyon cells of the honeybee mushroom body. Frontiers in systems neuroscience<\/em> 2<\/strong>, 3, doi:10.3389\/neuro.06.003.2008 (2008).<\/li>\n
  31. Fernandez, P. C., Locatelli, F. F., Person-Rennell, N., Deleo, G. & Smith, B. H. Associative conditioning tunes transient dynamics of early olfactory processing. The Journal of neuroscience : the official journal of the Society for Neuroscience<\/em> 29<\/strong>, 10191-10202, doi:10.1523\/JNEUROSCI.1874-09.2009 (2009).<\/li>\n
  32. Rath, L., Giovanni Galizia, C. & Szyszka, P. Multiple memory traces after associative learning in the honey bee antennal lobe. The European journal of neuroscience<\/em> 34<\/strong>, 352-360, doi:10.1111\/j.1460-9568.2011.07753.x (2011).<\/li>\n
  33. Akers, R. P. & Getz, W. M. Response of olfactory receptor neurons in honeybees to odorants and their binary mixtures. Journal of Comparative Physiology A<\/em> 173<\/strong>, 16 (1993).<\/li>\n
  34. Su, C. Y., Menuz, K., Reisert, J. & Carlson, J. R. Non-synaptic inhibition between grouped neurons in an olfactory circuit. Nature<\/em> 492<\/strong>, 66-71, doi:10.1038\/nature11712 (2012).<\/li>\n
  35. Stopfer, M., Bhagavan, S., Smith, B. H. & Laurent, G. Impaired odour discrimination on desynchronization of odour-encoding neural assemblies. Nature<\/em> 390<\/strong>, 70-74 (1997).<\/li>\n
  36. Froese, A., Szyszka, P. & Menzel, R. Effect of GABAergic inhibition on odorant concentration coding in mushroom body intrinsic neurons of the honeybee. Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology<\/em> 200<\/strong>, 183-195, doi:10.1007\/s00359-013-0877-8 (2014).<\/li>\n
  37. Bitterman, M. E., Menzel, R., Fietz, A. & Schafer, S. Classical conditioning of proboscis extension in honeybees (Apis mellifera). J Comp Psychol<\/em> 97<\/strong>, 107-119 (1983).<\/li>\n
  38. Farooqui, T., Robinson, K., Vaessin, H. & Smith, B. H. Modulation of early olfactory processing by an octopaminergic reinforcement pathway in the honeybee. The Journal of neuroscience : the official journal of the Society for Neuroscience<\/em> 23<\/strong>, 5370-5380 (2003).<\/li>\n
  39. Farooqui, T., Vaessin, H. & Smith, B. H. Octopamine receptors in the honeybee (Apis mellifera) brain and their disruption by RNA-mediated interference. Journal of insect physiology<\/em> 50<\/strong>, 701-713, doi:10.1016\/j.jinsphys.2004.04.014 (2004).<\/li>\n
  40. Chung, B. Y., Kilman, V. L., Keath, J. R., Pitman, J. L. & Allada, R. The GABA(A) receptor RDL acts in peptidergic PDF neurons to promote sleep in Drosophila. Current biology : CB<\/em> 19<\/strong>, 386-390, doi:10.1016\/j.cub.2009.01.040 (2009).<\/li>\n
  41. Hosie, A. M., Aronstein, K., Sattelle, D. B. & ffrench-Constant, R. H. Molecular biology of insect neuronal GABA receptors. Trends in neurosciences<\/em> 20<\/strong>, 578-583 (1997).<\/li>\n
  42. Ffrench-Constant, R. H., Mortlock, D. P., Shaffer, C. D., MacIntyre, R. J. & Roush, R. T. Molecular cloning and transformation of cyclodiene resistance in Drosophila: an invertebrate gamma-aminobutyric acid subtype A receptor locus. Proc Natl Acad Sci U S A<\/em> 88<\/strong>, 7209-7213 (1991).<\/li>\n
  43. Harvey, R. J., Chinchetru, M. A. & Darlison, M. G. Alternative splicing of a 51-nucleotide exon that encodes a putative protein kinase C phosphorylation site generates two forms of the chicken gamma-aminobutyric acidA receptor beta 2 subunit. J Neurochem<\/em> 62<\/strong>, 10-16 (1994).<\/li>\n
  44. Henderson, J. E., Soderlund, D. M. & Knipple, D. C. Characterization of a putative gamma-aminobutyric acid (GABA) receptor beta subunit gene from Drosophila melanogaster. Biochemical and biophysical research communications<\/em> 193<\/strong>, 474-482, doi:10.1006\/bbrc.1993.1648 (1993).<\/li>\n
  45. Aronstein, K. & Ffrench-Constant, R. Immunocytochemistry of a novel GABA receptor subunit Rdl in Drosophila melanogaster. Invertebrate neuroscience : IN<\/em> 1<\/strong>, 25-31 (1995).<\/li>\n
  46. Harrison, J. B. et al.<\/em> Immunocytochemical mapping of a C-terminus anti-peptide antibody to the GABA receptor subunit, RDL in the nervous system in Drosophila melanogaster. Cell and tissue research<\/em> 284<\/strong>, 269-278 (1996).<\/li>\n
  47. Jones, A. K. & Sattelle, D. B. The cys-loop ligand-gated ion channel superfamily of the honeybee, Apis mellifera. Invertebrate neuroscience : IN<\/em> 6<\/strong>, 123-132, doi:10.1007\/s10158-006-0026-y (2006).<\/li>\n
  48. Dupuis, J. P. et al.<\/em> Homomeric RDL and heteromeric RDL\/LCCH3 GABA receptors in the honeybee antennal lobes: two candidates for inhibitory transmission in olfactory processing. Journal of neurophysiology<\/em> 103<\/strong>, 458-468, doi:10.1152\/jn.00798.2009 (2010).<\/li>\n
  49. Ffrench-Constant, R. H. & Rocheleau, T. A. Drosophila gamma-aminobutyric acid receptor gene Rdl shows extensive alternative splicing. J Neurochem<\/em> 60<\/strong>, 2323-2326 (1993).<\/li>\n
  50. Glueck, S. B. Molecular evolution of Rdl in insects. PhD Dissertation Cornell University<\/em> (1998).<\/li>\n
  51. Wang, Y. et al.<\/em> Down-regulation of honey bee IRS gene biases behavior toward food rich in protein. PLoS genetics<\/em> 6<\/strong>, e1000896, doi:10.1371\/journal.pgen.1000896 (2010).<\/li>\n
  52. Wang, Y., Brent, C. S., Fennern, E. & Amdam, G. V. Gustatory perception and fat body energy metabolism are jointly affected by vitellogenin and juvenile hormone in honey bees. PLoS genetics<\/em> 8<\/strong>, e1002779, doi:10.1371\/journal.pgen.1002779 (2012).<\/li>\n
  53. Matsumoto, Y., Menzel, R., Sandoz, J. C. & Giurfa, M. Revisiting olfactory classical conditioning of the proboscis extension response in honey bees: A step toward standardized procedures. Journal of neuroscience methods<\/em> 211<\/strong>, 159-167, doi:10.1016\/j.jneumeth.2012.08.018 (2012).<\/li>\n
  54. Nowotny, T., Huerta, R., Abarbanel, H. D. & Rabinovich, M. I. Self-organization in the olfactory system: one shot odor recognition in insects. Biol Cybern<\/em> 93<\/strong>, 436-446, doi:10.1007\/s00422-005-0019-7 (2005).<\/li>\n
  55. Huerta, R., Nowotny, T., Garcia-Sanchez, M., Abarbanel, H. D. & Rabinovich, M. I. Learning classification in the olfactory system of insects. Neural computation<\/em> 16<\/strong>, 1601-1640, doi:10.1162\/089976604774201613 (2004).<\/li>\n
  56. Hammer, M. An identified neuron mediates the unconditioned stimulus in associative olfactory learning in honeybees. Nature<\/em> 366<\/strong>, 59-63 (1993).<\/li>\n
  57. Hammer, M. & Menzel, R. Multiple sites of associative odor learning as revealed by local brain microinjections of octopamine in honeybees. Learn Mem<\/em> 5<\/strong>, 146-156 (1998).<\/li>\n
  58. Nowotny, T. Flexible neuronal network simulation framework using code generation for NVidia\u00ae CUDA\u2122. BMC neuroscience<\/em> 12<\/strong>(Suppl 1): P239 (2011).<\/li>\n
  59. Mayer, M. S., Mankin, R. W. & Lemire, G. F. Quantitation of the Insect Electroantennogram – Measurement of Sensillar Contributions, Elimination of Background Potentials, and Relationship to Olfactory Sensation. Journal of insect physiology<\/em> 30<\/strong>, 757-763 (1984).<\/li>\n
  60. Sakurai, T. et al.<\/em> A single sex pheromone receptor determines chemical response specificity of sexual behavior in the silkmoth Bombyx mori. PLoS genetics<\/em> 7<\/strong>, e1002115, doi:10.1371\/journal.pgen.1002115 (2011).<\/li>\n
  61. Larsson, M. C. et al.<\/em> Or83b encodes a broadly expressed odorant receptor essential for Drosophila olfaction. Neuron<\/em> 43<\/strong>, 703-714, doi:10.1016\/j.neuron.2004.08.019 (2004).<\/li>\n
  62. Kanzaki, R., Minegishi, R., Namiki, S. & Ando, N. Insect-machine hybrid system for understanding and evaluating sensory-motor control by sex pheromone in Bombyx mori. Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology<\/em> 199<\/strong>, 1037-1052, doi:10.1007\/s00359-013-0832-8 (2013).<\/li>\n
  63. Martinez, D., Arhidi, L., Demondion, E., Masson, J. B. & Lucas, P. Using insect electroantennogram sensors on autonomous robots for olfactory searches. Journal of visualized experiments : JoVE<\/em>, doi:10.3791\/51704 (2014).<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    The following bibliography highlights research underpinning or related to the project. Murlis, J., Elkinton, J. S. & Carde, R. T. Odor Plumes and How Insects Use Them. Annu Rev Entomol 37, 505-532 (1992). Baker, T. C., Fadamiro, H. Y. & Cosse, A. A. Moth uses fine tuning for odour resolution. Nature 393, 530-530 (1998). Fadamiro, … Continue reading References<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[],"_links":{"self":[{"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/posts\/61"}],"collection":[{"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/comments?post=61"}],"version-history":[{"count":8,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/posts\/61\/revisions"}],"predecessor-version":[{"id":356,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/posts\/61\/revisions\/356"}],"wp:attachment":[{"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/media?parent=61"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/categories?post=61"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/odor-objects.inf.sussex.ac.uk\/wordpress\/index.php\/wp-json\/wp\/v2\/tags?post=61"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}