Unlabelled: Here, we studied neural correlates of orientation-contrast-based saliency in the optic tectum (OT) of barn owls. Neural responses in the intermediate/deep layers of the OT were recorded from lightly anesthetized owls confronted with arrays of bars in which one bar (the target) was orthogonal to the remaining bars (the distractors). Responses to target bars were compared with responses to distractor bars in the receptive field (RF). Initially, no orientation-contrast sensitivity was observed. However, if the position of the target bar in the array was randomly shuffled across trials so that it occasionally appeared in the RF, then such sensitivity emerged. The effect started to become significant after three or four positional changes of the target bar and strengthened with additional trials. Our data further suggest that this effect arises due to specific adaptation to the stimulus in the RF combined with suppression from the surround. By jittering the position of the bar inside the RF across trials, we demonstrate that the adaptation has two components, one position specific and one orientation specific. The findings give rise to the hypothesis that barn owls, by active scanning of the scene, can induce adaptation of the tectal circuitry to the common orientation and thus achieve a "pop-out" of rare orientations. Such a model is consistent with several behavioral observations in owls and may be relevant to other visual features and species.
Significance Statement: Natural scenes are often characterized by a dominant orientation, such as the scenery of a pine forest or the sand dunes in a windy desert. Therefore, orientation that contrasts the regularity of the scene is perceived salient for many animals as a means to break camouflage. By actively moving the scene between each trial, we show here that neurons in the retinotopic map of the barn owl's optic tectum specifically adapt to the common orientation, giving rise to preferential representation of odd orientations. Based on this, we suggest a new mechanism for orientation-based camouflage breaking that links active scanning of scenes with neural adaptation. This mechanism may be relevant to pop-out in other species and visual features.
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http://dx.doi.org/10.1523/JNEUROSCI.3339-15.2016 | DOI Listing |
J Neurophysiol
December 2024
Dept. of Biol., University of Massachusetts Amherst, , Amherst, MA.
Lab rodent species commonly used to study the visual system and its development (hamsters, rats, and mice) are crepuscular/nocturnal, altricial, and possess simpler visual systems than carnivores and primates. To widen the spectra of studied species, here we introduce an alternative model, the Chilean degu (). This diurnal, precocial Caviomorph rodent has a cone enriched, well-structured retina, and well-developed central visual projections.
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December 2024
Institute of Coastal Environmental Pollution Control, College of Environmental Science and Engineering, Key Laboratory of Marine Environment and Ecology, Ministry of Education, Ocean University of China, Qingdao 266100, China; Sanya Oceanographic Institution, Ocean University of China, Sanya 57200, China.
The widespread use of plasticizers like phthalate esters (PAEs) has led to environmental and health concerns. The neurobehavioral toxicity of these compounds in marine environments, particularly regulated by the "brain-gut" axis, remains unclear, especially concerning wild demersal fish of high ecological value. Our investigation into the behavioral effects of three common PAEs, i.
View Article and Find Full Text PDFExp Eye Res
January 2025
Department of Ophthalmology & Visual Science, Eye & ENT Hospital, Shanghai Medical College, Fudan University, Shanghai, 200032, China; State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, 200031, China; NHC Key Laboratory of Myopia and Related Eye Diseases, Chinese Academy of Medical Sciences, and Shanghai Key Laboratory of Visual Impairment and Restoration (Fudan University), Shanghai, 200032, China. Electronic address:
Normal perception of visual information relies not only on the quantity and quality of retinal ganglion cells (RGCs), but also on the integrity of the visual pathway, within which RGC central projection predominates. However, the exact changes of RGC central projection under particular pathological conditions remain to be elucidated. Here, we report a whole-brain clearing method modified from iDISCO for 3D visualization of RGC central projection.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
November 2024
Center for Regenerative Therapies at TU Dresden(CRTD), Dresden, Germany.
J Neurophysiol
January 2025
Werner Reichardt Centre for Integrative Neuroscience, University of Tübingen, Tübingen, Germany.
We normally perceive a stable visual environment despite eye movements. To achieve such stability, visual processing integrates information across a given saccade, and laboratory hallmarks of such integration are robustly observed by presenting brief perisaccadic visual probes. In one classic phenomenon, probe locations are grossly mislocalized.
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