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      Parallel processing in the honeybee olfactory pathway: structure, function, and evolution

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          Abstract

          Animals face highly complex and dynamic olfactory stimuli in their natural environments, which require fast and reliable olfactory processing. Parallel processing is a common principle of sensory systems supporting this task, for example in visual and auditory systems, but its role in olfaction remained unclear. Studies in the honeybee focused on a dual olfactory pathway. Two sets of projection neurons connect glomeruli in two antennal-lobe hemilobes via lateral and medial tracts in opposite sequence with the mushroom bodies and lateral horn. Comparative studies suggest that this dual-tract circuit represents a unique adaptation in Hymenoptera. Imaging studies indicate that glomeruli in both hemilobes receive redundant sensory input. Recent simultaneous multi-unit recordings from projection neurons of both tracts revealed widely overlapping response profiles strongly indicating parallel olfactory processing. Whereas lateral-tract neurons respond fast with broad (generalistic) profiles, medial-tract neurons are odorant specific and respond slower. In analogy to “what-” and “where” subsystems in visual pathways, this suggests two parallel olfactory subsystems providing “what-” (quality) and “when” (temporal) information. Temporal response properties may support across-tract coincidence coding in higher centers. Parallel olfactory processing likely enhances perception of complex odorant mixtures to decode the diverse and dynamic olfactory world of a social insect.

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          The online version of this article (doi:10.1007/s00359-013-0821-y) contains supplementary material, which is available to authorized users.

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          Most cited references113

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          Is Open Access

          The Neural Architecture of the Language Comprehension Network: Converging Evidence from Lesion and Connectivity Analyses

          While traditional models of language comprehension have focused on the left posterior temporal cortex as the neurological basis for language comprehension, lesion and functional imaging studies indicate the involvement of an extensive network of cortical regions. However, the full extent of this network and the white matter pathways that contribute to it remain to be characterized. In an earlier voxel-based lesion-symptom mapping analysis of data from aphasic patients (Dronkers et al., 2004), several brain regions in the left hemisphere were found to be critical for language comprehension: the left posterior middle temporal gyrus, the anterior part of Brodmann's area 22 in the superior temporal gyrus (anterior STG/BA22), the posterior superior temporal sulcus (STS) extending into Brodmann's area 39 (STS/BA39), the orbital part of the inferior frontal gyrus (BA47), and the middle frontal gyrus (BA46). Here, we investigated the white matter pathways associated with these regions using diffusion tensor imaging from healthy subjects. We also used resting-state functional magnetic resonance imaging data to assess the functional connectivity profiles of these regions. Fiber tractography and functional connectivity analyses indicated that the left MTG, anterior STG/BA22, STS/BA39, and BA47 are part of a richly interconnected network that extends to additional frontal, parietal, and temporal regions in the two hemispheres. The inferior occipito-frontal fasciculus, the arcuate fasciculus, and the middle and inferior longitudinal fasciculi, as well as transcallosal projections via the tapetum were found to be the most prominent white matter pathways bridging the regions important for language comprehension. The left MTG showed a particularly extensive structural and functional connectivity pattern which is consistent with the severity of the impairments associated with MTG lesions and which suggests a central role for this region in language comprehension.
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            Intensity versus identity coding in an olfactory system.

            We examined the encoding and decoding of odor identity and intensity by neurons in the antennal lobe and the mushroom body, first and second relays, respectively, of the locust olfactory system. Increased odor concentration led to changes in the firing patterns of individual antennal lobe projection neurons (PNs), similar to those caused by changes in odor identity, thus potentially confounding representations for identity and concentration. However, when these time-varying responses were examined across many PNs, concentration-specific patterns clustered by identity, resolving the apparent confound. This is because PN ensemble representations changed relatively continuously over a range of concentrations of each odorant. The PNs' targets in the mushroom body-Kenyon cells (KCs)-had sparse identity-specific responses with diverse degrees of concentration invariance. The tuning of KCs to identity and concentration and the patterning of their responses are consistent with piecewise decoding of their PN inputs over oscillation-cycle length epochs.
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              Olfactory network dynamics and the coding of multidimensional signals.

                Author and article information

                Contributors
                +49-931-318-4306 , +49-931-318-4309 , roessler@biozentrum.uni-wuerzburg.de
                Journal
                J Comp Physiol A Neuroethol Sens Neural Behav Physiol
                J. Comp. Physiol. A Neuroethol. Sens. Neural. Behav. Physiol
                Journal of Comparative Physiology. A, Neuroethology, Sensory, Neural, and Behavioral Physiology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0340-7594
                1432-1351
                23 April 2013
                23 April 2013
                2013
                : 199
                : 981-996
                Affiliations
                Behavioral Physiology and Sociobiology (Zoology II), Biozentrum, University of Würzburg, Am Hubland, 97074 Würzburg, Germany
                Article
                821
                10.1007/s00359-013-0821-y
                3824823
                23609840
                d0e13755-3173-4d59-9111-c5e1d7f0175b
                © The Author(s) 2013

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

                History
                : 24 January 2013
                : 10 April 2013
                : 11 April 2013
                Categories
                Review
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2013

                Neurology
                antennal lobe,glomeruli,projection neurons,mushroom bodies,multi-unit recording
                Neurology
                antennal lobe, glomeruli, projection neurons, mushroom bodies, multi-unit recording

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