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    <title>Visual Neuroscience - Current Issue</title>
    <link>http://journals.cambridge.org/action/displayJournal?jid=VNS</link>
    <description>Visual Neuroscience, Volume 25 Issue 04&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;table border='0'&gt;&lt;tr&gt;&lt;td&gt; Visual Neuroscience  is an international journal devoted to the publication of high-quality reports of experimental and theoretical research in basic visual neuroscience. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of contemporary research on neural mechanisms of vision. Contributions deal with molecular, cellular and systems-level processes in both vertebrate and invertebrate species. Studies based exclusively on clinical, psychophysiological or behavioral data are included if they are designed to address questions concerning neural mechanisms of vision.&lt;/td&gt;&lt;td&gt; &lt;a href='http://journals.cambridge.org/jid_VNS'&gt;&lt;img src='http://journals.cambridge.org/cover_images/VNS/VNS.jpg' align='right'  border='1' alt='Visual Neuroscience'/&gt;&lt;/a&gt;&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</description>
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      <title>Journals Cambridge Online</title>
      <url>http://journals.cambridge.org/images/logo_6699CC_large.gif</url>
      <link>http://journals.cambridge.org</link>
      <description>Journals Cambridge Online</description>
    </image>
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      <title>Volume 25 Issue 04</title>
      <link>http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04</link>
      <description>Visual Neuroscience, Volume 25 Issue 04&lt;br /&gt;&lt;br /&gt;&lt;br /&gt;&lt;table border='0'&gt;&lt;tr&gt;&lt;td&gt; Visual Neuroscience  is an international journal devoted to the publication of high-quality reports of experimental and theoretical research in basic visual neuroscience. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of contemporary research on neural mechanisms of vision. Contributions deal with molecular, cellular and systems-level processes in both vertebrate and invertebrate species. Studies based exclusively on clinical, psychophysiological or behavioral data are included if they are designed to address questions concerning neural mechanisms of vision.&lt;/td&gt;&lt;td&gt; &lt;a href='http://journals.cambridge.org/jid_VNS'&gt;&lt;img src='http://journals.cambridge.org/cover_images/VNS/VNS.jpg' align='right'  border='1' alt='Visual Neuroscience'/&gt;&lt;/a&gt;&lt;/td&gt;&lt;/tr&gt;&lt;/table&gt;</description>
      <pubDate>Mon, 30 Jun 2008 23:00:00 GMT</pubDate>
      <guid>http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04</guid>
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      <title>Synaptic vesicle dynamics in mouse rod bipolar cells</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176764</link>
      <description>Research Articles&lt;br /&gt;QUN-FANG WAN, ALEJANDRO VILA, ZHEN-YU ZHOU, RUTH HEIDELBERGER,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 523-533&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176764'&gt;Abstract&lt;/a&gt;&lt;br /&gt;To better understand synaptic signaling at the mammalian rod bipolar cell terminal and pave the way for applying genetic approaches to the study of visual information processing in the mammalian retina, synaptic vesicle dynamics and intraterminal calcium were monitored in terminals of acutely isolated mouse rod bipolar cells and the number of ribbon-style active zones quantified. We identified a releasable pool, corresponding to a maximum of  7 s. The presence of a smaller, rapidly releasing pool and a small, fast component of refilling was also suggested. Following calcium channel closure, membrane surface area was restored to baseline with a time constant that ranged from 2 to 21 s depending on the magnitude of the preceding Ca2+ transient. In addition, a brief, calcium-dependent delay often preceded the start of onset of membrane recovery. Thus, several aspects of synaptic vesicle dynamics appear to be conserved between rod-dominant bipolar cells of fish and mammalian rod bipolar cells. A major difference is that the number of vesicles available for release is significantly smaller in the mouse rod bipolar cell, both as a function of the total number per neuron and on a per active zone basis.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176764</guid>
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      <title>The maintained discharge of rat retinal ganglion cells</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176716</link>
      <description>Research Articles&lt;br /&gt;DANIEL K. FREEMAN, WALTER F. HEINE, CHRISTOPHER L. PASSAGLIA,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 535-548&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176716'&gt;Abstract&lt;/a&gt;&lt;br /&gt;Action potentials were recorded from rat retinal ganglion cell fibers in the presence of a uniform field, and the maintained discharge pattern was characterized. Spike trains recorded under ketamine xylazine. The majority of cells had multimodal interval distributions, with the first peak in the range of 25.0 0.97). Both ON and OFF cells show serial correlations between adjacent interspike intervals, while ON cells also showed second-order correlations. Cells with multimodal interval distribution showed a strong peak at high frequencies in the power spectra in the range of 28.9 41.4 Hz. Oscillations were present under both anesthetic conditions and persisted in the dark at a slightly lower frequency, implying that the oscillations are generated independent of any light stimulus but can be modulated by light level. The oscillation frequency varied slightly between cells of the same type and in the same eye, suggesting that multiple oscillatory generating mechanisms exist within the retina. Cells with high-frequency oscillations were described well by an integrate-and-fire model with the input consisting of Gaussian noise plus a sinusoid where the phase was jittered randomly to account for the bandwidth present in the oscillations.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176716</guid>
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      <title>Comparative visual function in elasmobranchs: Spatial arrangement and ecological correlates of photoreceptor and ganglion cell distributions</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176740</link>
      <description>Research Articles&lt;br /&gt;LENORE LITHERLAND, SHAUN P. COLLIN,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 549-561&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176740'&gt;Abstract&lt;/a&gt;&lt;br /&gt;The topographic analysis of retinal ganglion and photoreceptor cell distributions yields valuable information for assessing the visual capabilities and behavioral ecology of vertebrates. This study examines whole-mounted retinas of four elasmobranch species, the ornate wobbegong, Orectolobus ornatus; the whitetip reef shark, Triaenodon obesus; the epaulette shark, Hemiscyllium ocellatum; and the east Australia shovelnose ray, Aptychotrema rostrata, for regional specializations mediating zones of improved visual ability. These species represent a range of lifestyles: benthic, mid-water, diurnal, and nocturnal. Both photoreceptors (visualized using differential interference contrast optics) and ganglion cells (stained with cresyl violet) in the retina are extensively sampled, and their spatial distribution is found to be nonuniform, exhibiting areae or   In general, the topographic distributions of both cell populations are in register and match well with respect to the location of regions of high density. However, the location of peaks in rod and cone densities can vary within a retina, indicating that preferential sampling of different regions of the visual field may occur in photopic and scotopic vision. Anatomical measures of the optical limits of resolving power, indicated by intercone spacing, range from 3.8 to 13.1 cycles/deg. Spatial limits of resolving power, calculated from ganglion cell spacing, range from 2.6 to 4.3 cycles/deg. Summation ratios, assessed by direct comparison of cell densities of photoreceptors (input cells) and ganglion cells (output cells), at more than 150 different loci across the retina, show topographic differences in signal convergence (ranging from 25:1 to over 70:1). Species-specific retinal specializations strongly correlate to the habitat and feeding behavior of each species.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176740</guid>
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      <title>Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176776</link>
      <description>Research Articles&lt;br /&gt;JUNGYEON WON, RICHARD S. SMITH, NEAL S. PEACHEY, JIANG WU, WANDA L. HICKS, JÜRGEN K. NAGGERT, PATSY M. NISHINA,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 563-574&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176776'&gt;Abstract&lt;/a&gt;&lt;br /&gt;A 4 base pair deletion in a splice donor site of the Mfrp (membrane-type frizzled-related protein) gene, herein referred to as Mfrprd6/rd6, is predicted to lead to the skipping of exon 4 and photoreceptor degeneration in retinal degeneration 6 (rd6) mutant mice. Little, however, is known about the function of the protein or how the mutation causes the degenerative retinal phenotype. Here we examine ultrastructural changes in the retina of Mfrprd6/rd6 mice to determine the earliest effects of the mutation. We also extend the reported observations of the expression pattern of the dicistronic Mfrp/C1qtnf5 message and the localization of these and other retinal pigment epithelium (RPE) and retinal proteins during development and assess the ability of RPE cells to phagocytize outer segments (OSs) in mutant and wild-type (WT) mice. At the ultrastructural level, OSs do not develop normally in Mfrprd6/rd6 mutants. They are disorganized and become progressively shorter as mutant mice age. Additionally, there are focal areas in which there is a reduction of apical RPE microvilli. At P25, the rod electroretinogram (ERG) a-wave of Mfrprd6/rd6 mice is reduced in amplitude by ~50% as are ERG components generated by the RPE. Examination of  -catenin localization and Fos and Tcf-1 expression, intermediates of the canonical Wnt pathway, showed that they were not different between mutant and WT mice, suggesting that MFRP may operate through an alternative pathway. Finally, impaired OS phagocytosis was observed in Mfrprd6/rd6 mice both in standard ambient lighting conditions and with bright light exposure when compared to WT controls.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176776</guid>
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      <title>Measurement of macular pigment optical density and distribution using the steady-state visual evoked potential</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176728</link>
      <description>Research Articles&lt;br /&gt;ANTHONY G. ROBSON, NEIL R.A. PARRY,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 575-583&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176728'&gt;Abstract&lt;/a&gt;&lt;br /&gt;The purpose of this study was to specify isoluminance at different retinal eccentricities and to characterize macular pigment optical density (MPOD) and distribution using the steady-state visual evoked potential (VEP). Red green (B/G) gratings were generated within two circular stimulus fields (radius = 0.55 or 1.1 deg) and within four annular fields (maximum mean radius = 6.0 deg) on a color monitor. Temporal frequency was 15 Hz. Isoluminance was determined for each stimulus using minimum flicker photometry. Steady-state onset offset VEPs were recorded to the same annular stimuli as the luminance ratio between adjacent chromatic components was changed from 0.25 to 0.85 in 11 automated steps (0.5 representing photometric isoluminance). Fourier analysis showed that the power of the first harmonic was minimized at the isoluminant ratio specific to each subject. Relative OD was computed by comparing the isoluminant ratio at any location with that for the most eccentric annulus. To compensate for the broadband characteristics of the monitor, OD values were corrected according to minimum flicker measurements made through known concentrations of carotenoid solution. MPOD was additionally measured using minimum motion photometry.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176728</guid>
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      <title>A common contrast pooling rule for suppression within and between the eyes</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176752</link>
      <description>Research Articles&lt;br /&gt;TIM S. MEESE, KIRSTEN L. CHALLINOR, ROBERT J. SUMMERS,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 585-601&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176752'&gt;Abstract&lt;/a&gt;&lt;br /&gt;Recent work has revealed multiple pathways for cross-orientation suppression in cat and human vision. In particular, ipsiocular and interocular pathways appear to assert their influence before binocular summation in human but have different (1) spatial tuning, (2) temporal dependencies, and (3) adaptation after-effects. Here we use mask components that fall outside the excitatory passband of the detecting mechanism to investigate the rules for pooling multiple mask components within these pathways. We measured psychophysical contrast masking functions for vertical 1 cycle/deg sine-wave gratings in the presence of left or right oblique (  16%. We tested contrast gain control models involving two types of contrast combination on the denominator: (1) spatial pooling of the mask after a local nonlinearity (to calculate either root mean square contrast or energy) and (2)   (Holmes   Meese, 2004, Journal of Vision 4, 1080 1089), involving the linear sum of the mask component contrasts. Monoptic and dichoptic masking were typically better fit by the spatial pooling models, but binocular masking was not: it demanded strict linear summation of the Michelson contrast across mask orientation. Another scheme, in which suppressive pooling followed compressive contrast responses to the mask components (e.g., oriented cortical cells), was ruled out by all of our data. We conclude that the different processes that underlie monoptic and dichoptic masking use the same type of contrast pooling within their respective suppressive fields, but the effects do not sum to predict the binocular case.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176752</guid>
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      <title>Recognition of facial emotion in low vision: A flexible usage of facial features</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176704</link>
      <description>Research Articles&lt;br /&gt;MURIEL BOUCART, JEAN-FRANÇOIS DINON, PASCAL DESPRETZ, THOMAS DESMETTRE, KATRINE HLADIUK, AUDE OLIVA,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 603-609&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176704'&gt;Abstract&lt;/a&gt;&lt;br /&gt;Age-related macular degeneration (AMD) is a major cause of visual impairment in people older than 50 years in Western countries, affecting essential tasks such as reading and face recognition. Here we investigated the mechanisms underlying the deficit in recognition of facial expressions in an AMD population with low vision. Pictures of faces displaying different emotions with the mouth open or closed were centrally displayed for 300 ms. Participants with AMD with low acuity (mean 20/200) and normally sighted age-matched controls performed one of two emotion tasks: detecting whether a face had an expression or not (expressive/non expressive (EXNEX) task) or categorizing the facial emotion as happy, angry, or neutral (categorization of expression (CATEX) task). Previous research has shown that healthy observers are mainly using high spatial frequencies in an EXNEX task while performance at a CATEX task was preferentially based on low spatial frequencies. Due to impaired processing of high spatial frequencies in central vision, we expected and observed that AMD participants failed at deciding whether a face was expressive or not but categorized normally the emotion of the face (e.g., happy, angry, neutral). Moreover, we observed that AMD participants mostly identified emotions using the lower part of the face (mouth). Accuracy did not differ between the two tasks for normally sighted observers. The results indicate that AMD participants are able to identify facial emotion but must base their decision mainly on the low spatial frequencies, as they lack the perception of finer details.</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176704</guid>
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      <title>Metacontrast, target recovery, and the magno- and parvocellular systems: A reply to the perspective</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176692</link>
      <description>Letter&lt;br /&gt;Haluk Öğmen, Gopathy Purushothaman, Bruno G. Breitmeyer,  &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 611-616&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176692'&gt;Abstract&lt;/a&gt;</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176692</guid>
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      <title>Free Color Online in Cambridge University Press Journals</title>
      <link>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176788</link>
      <description>Announcement&lt;br /&gt; &lt;br /&gt;&lt;a href='http://journals.cambridge.org/jid_VNS'&gt;Visual Neuroscience&lt;/a&gt;, &lt;a href='http://journals.cambridge.org/action/displayIssue?jid=VNS&amp;volumeId=25&amp;issueId=04'&gt;Volume 25 Issue 04&lt;/a&gt; , pp 617-617&lt;br /&gt;&lt;br /&gt;&lt;a href='http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176788'&gt;Abstract&lt;/a&gt;</description>
      <guid>http://journals.cambridge.org/action/displayAbstract?fromPage=online&amp;aid=2176788</guid>
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