Attentional weighting: a possible account of visual field asymmetries in visual search?

Several previous visual search studies measuring reaction times have demonstrated scanning biases across the visual field (i.e. a tendency to begin a serial search in a particular region of space). In the present study, we measured visual discrimination thresholds for a target presented amongst distractors using displays that were short enough to greatly reduce the potential for serial (i.e. scanning) search. For both a motion and orientation task, subjects' performance was significantly better when the target appeared in the inferior, as compared to the superior, visual field (no differences were observed between left and right visual fields). These findings suggest that subjects may divide attention unevenly across the visual field when searching for a target amongst distractors, a phenomenon we refer to as 'attentional weighting'. To rule out the possibility that these visual field asymmetries were sensory in nature, thresholds were also measured for conditions in which subjects' attention was directed to the location of the target stimulus, either because it was presented alone in the display or because a spatial cue directed subjects' attention to the location of that target presented amongst distractors. Under these conditions, visual field asymmetries were smaller (or non-existent), suggesting that sensory factors (such as crowding) are unlikely to account for our results. In addition, analyses of set-size effects (obtained by comparing thresholds for a single target vs. the target presented amongst distractors) could be accounted for by an unlimited capacity model, suggesting that multiple stimuli can be processed simultaneously without any limitations at an early stage of sensory processing. Taken together, these findings suggest the possible existence of biases in attentional weighting at a late stage of processing. The bias appears to favor the inferior visual field, which may arise from the fact that there is more ecologically-relevant information in this region of space.     

How does the brain sustain a visual percept?

Perception involves the processing of sensory stimuli and their translation into conscious experience. A novel percept can, once synthesized, be maintained or discarded from awareness. We used event-related functional magnetic resonance imaging to separate the neural responses associated with the maintenance of a percept, produced by single-image, random-dot stereograms, from the response evoked at the onset of the percept. The latter was associated with distributed bilateral activation in the posterior thalamus and regions in the occipito-temporal, parietal and frontal cortices. In contrast, sustained perception was associated with activation of the pre-frontal cortex and hippocampus. This observation suggests that sustaining a visual percept involves neuroanatomical systems which are implicated in memory function and which are distinct from those engaged during perceptual synthesis.     

Synchronized oscillations in the visual cortex — a synergetic model

 We present an oscillator network model for the synchronization of oscillatory neuronal activity underlying visual processing. The single neuron is modeled by means of a limit cycle oscillator with an eigenfrequency corresponding to visual stimulation. The eigenfrequency may be time dependent. The mutual coupling strengths are unsymmetrical and activity dependent, and they scatter within the network. Synchronized clusters (groups) of neurons emerge in the network due to the visual stimulation. The different clusters correspond to different visual stimuli. There is no limitation of the number of stimuli. Distinct clusters do not perturb each other, although the coupling strength between all model neurons is of the same order of magnitude. Our analysis is not restricted to weak coupling strength. The scatter of the couplings causes shifts of the cluster frequencies. The model’s behavior is compared with the experimental findings. The coupling mechanism is extended in order to model the influence of bicucullin upon the neural network. We additionally investigate repulsive couplings, which lead to constant phase differences between clusters of the same frequency. Finally, we consider the problem of selective attention from the viewpoint of our model. Received: 15 February 1995/Accepted in revised form: 18 July 1995     

Is slowness a learning principle of the visual cortex?

Slow feature analysis is an algorithm for extracting slowly varying features from a quickly varying signal. It has been shown in network simulations on one-dimensional stimuli that visual invariances to shift and other transformations can be learned in an unsupervised fashion based on slow feature analysis. More recently, we have shown that slow feature analysis applied to image sequences generated from natural images using a range of spatial transformations results in units that share many properties with complex and hypercomplex cells of the primary visual cortex. We find cells responsive to Gabor stimuli with phase invariance, sharpened or widened orientation or frequency tuning, secondary response lobes, end-stopping, and cells selective for direction of motion. These results indicate that slowness may be an important principle of self-organization in the visual cortex.     

Does food play a prominent role in visual attention to disgusting stimuli?

Journal of Ethology - Disgust is a basic emotion which protects individuals from potential contamination. It is hypothesized that disgust evolved primarily as a mechanism against oral contamination...     

What visual information is used for navigation around obstacles in a cluttered environment?

The goal of this study was to determine what visual information is used to navigate around barriers in a cluttered terrain. Twelve traffic pylons were arranged randomly in a 4.55 x 3.15 m travel area: there were 20 different arrangements. For each arrangement, individuals (N = 6) were positioned in 1 of 3 locations on the outside border with their eyes closed: on verbal command they were instructed to open their eyes and quickly go to 1 of 2 specified goals (2 vertical posts defining a door) located on one edge of the travel area. The movement of the body was tracked using the OPTOTRAK system, with the IREDS placed on a collar worn by the subjects. Experimental data of travel path chosen were compared with those predicted by models that incorporated different types of visual information to control path trajectory. The 6 models basically use 2 different strategies for route selection: reactive control based on visual input about the obstacle encountered in the line-of-sight travel path (Model # 1) and path planning based on different visual information (Model # 2, 3, 4, 5, and 6). The models that involve path planning are grouped into 2 categories: models 2, 3, 4, and 5 need detailed geometrical configuration of the obstacles to plan a route while model 6 plans a route based on identifying and avoiding a cluster of obstacles in the travel path. Two measures were used to compare model performance with the actual travel path: the difference in area between predicted and actual travel path and the number of trials that accurately predicted the number of turns during travel. The results suggest that route selection is not based on reactive control, but does involve path planning. The model that best predicts the travel paths taken by the individuals uses visual information about cluster of obstacles and identification of safe corridors to plan a route.     

Ovariectomy and 17β-estradiol replacement in rats and mice: a visual demonstration

Estrogens are a family of female sexual hormones with an exceptionally wide spectrum of effects. When rats and mice are used in estrogen research they are commonly ovariectomized in order to ablate the rapidly cycling hormone production, replacing the 17β-estradiol exogenously. There is, however, lack of consensus regarding how the hormone should be administered to obtain physiological serum concentrations. This is crucial since the 17β-estradiol level/administration method profoundly influences the experimental results. We have in a series of studies characterized the different modes of 17β-estradiol administration, finding that subcutaneous silastic capsules and per-oral nut-cream Nutella are superior to commercially available slow-release pellets (produced by the company Innovative Research of America) and daily injections in terms of producing physiological serum concentrations of 17β-estradiol. Amongst the advantages of the nut-cream method, that previously has been used for buprenorphine administration, is that when used for estrogen administration it resembles peroral hormone replacement therapy and is non-invasive. The subcutaneous silastic capsules are convenient and produce the most stable serum concentrations. This video article contains step-by-step demonstrations of ovariectomy and 17β-estradiol hormone replacement by silastic capsules and peroral Nutella in rats and mice, followed by a discussion of important aspects of the administration procedures.     

Visual system: prostriata - a visual area off the beaten path

Recent work establishes that Prostriata, a little-studied area of the visual cortex neighboring V1, has distinct but hybrid visual properties which are suggestive of an unsuspected role in the rapid analysis and integration of peripheral visual stimuli.     

Through a barn owl’s eyes: interactions between scene content and visual attention

In this study we investigated visual attention properties of freely behaving barn owls, using a miniature wireless camera attached to their heads. The tubular eye structure of barn owls makes them ideal subjects for this research since it limits their eye movements. Video sequences recorded from the owl’s point of view capture part of the visual scene as seen by the owl. Automated analysis of video sequences revealed that during an active search task, owls repeatedly and consistently direct their gaze in a way that brings objects of interest to a specific retinal location (retinal fixation area). Using a projective model that captures the geometry between the eye and the camera, we recovered the corresponding location in the recorded images (image fixation area). Recording in various types of environments (aviary, office, outdoors) revealed significant statistical differences of low level image properties at the image fixation area compared to values extracted at random image patches. These differences are in agreement with results obtained in primates in similar studies. To investigate the role of saliency and its contribution to drawing the owl’s attention, we used a popular bottom-up computational model. Saliency values at the image fixation area were typically greater than at random patches, yet were only 20% out of the maximal saliency value, suggesting a top-down modulation of gaze control.     

Interaction with transducin depletes metarhodopsin III: a regulated retinal storage in visual signal transduction?

In the phototransduction pathway of rhodopsin, the metarhodopsin (Meta) III retinal storage form arises from the active G-protein binding Meta II by a slow spontaneous reaction through the Meta I precursor or by light absorption and photoisomerization, respectively. Meta III is a side product of the Meta II decay path and holds its retinal in the original binding site, with the Schiff base bond to the apoprotein reprotonated as in the dark ground state. It thus keeps the retinal away from the regeneration pathway in which the photolyzed all-trans-retinal is released. This study was motivated by our recent observation that Meta III remains stable for hours in membranes devoid of regulatory proteins, whereas it decays much more rapidly in situ. We have now explored the possibility of regulated formation and decay of Meta III, using intrinsic opsin tryptophan fluorescence and UV-visible and Fourier transform infrared spectroscopy. We find that a rapid return of Meta III into the regeneration pathway is triggered by the G-protein transducin (G(t)). Depletion of the retinal storage is initiated by a novel direct bimolecular interaction of G(t) with Meta III, which was previously considered inactive. G(t) thereby induces the transition of Meta III into Meta II, so that the retinylidene bond to the apoprotein can be hydrolyzed, and the retinal can participate again in the normal retinoid cycle. Beyond the potential significance for retinoid metabolism, this may provide the first example of a G-protein-catalyzed conversion of a receptor.     

Emergence of orientation-selective inhibition in the primary visual cortex: a Bayes–Markov computational model

The recent consensus is that virtually all aspects of response selectivity exhibited by the primary visual cortex are either created or sharpened by cortical inhibitory interneurons. Experimental studies have shown that there are cortical inhibitory cells that are driven by geniculate cells and that, like their cortical excitatory counterparts, are orientation selective, though less sharply tuned. The main goal of this article is to demonstrate how orientation-selective inhibition might be created by the circuitry of the primary visual cortex (striate cortex, V1) from its nonoriented geniculate inputs. To fulfill this goal, first, a Bayes–Markov computational model is developed for the V1 area dedicated to foveal vision. The developed model consists of three parts: (i) a two-layered hierarchical Markov random field that is assumed to generate the activity patterns of the geniculate and cortical inhibitory cells, (ii) a Bayesian computational goal that is formulated based on the maximum a posteriori (MAP) estimation principle, and (iii) an iterative, deterministic, parallel algorithm that leads the cortical circuitry to achieve its assigned computational goal. The developed model is not fully LGN driven and it is not implementable by the neural machinery of V1. The model, then, is transformed into a fully LGN-driven and physiologically plausible form. Computer simulation is used to demonstrate the performance of the developed models.     

Shades of Déjerine--forging a causal link between the visual word form area and reading

In 1892, the French neurologist Jules Déjerine suggested that pure alexia resulted from an occipital lesion that selectively disconnected visual input from a region of the brain that housed "optical images of words." In this issue of Neuron, Gaillard and colleagues offer evidence consistent with Déjerine's proposal and provide new insights to the functional role of the "visual word form area."     

Superposition and scattering of visual fields in a compound,double eye—II. Stimulation sequences for different distances in a stomatopod from a bright habitat

• 1.1. The inputs deriving from a point light moving in front of a column of ommatidia are plotted by a computer.
• 2.2. Overlap of visual fields causes one main, central maximum surrounded by smaller maxima intercalated by minima.
• 3.3. With increasing distance of the point from the eye the central maximum increases.
• 4.4. Ommatidia in each half of the eye are stimulated sequentially in two groups. Stimulation sequences are parallel between the two halves of the eye.
• 5.5. We postulate an integrative mechanism for processing the succession of simultaneous inputs and hypothesize that the animal derives information about speed and distance from that mechanism.

     

Symmetries,non-Euclidean metrics,and patterns in a Swift–Hohenberg model of the visual cortex

The aim of this work is to investigate the effect of the shift-twist symmetry on pattern formation processes in the visual cortex. First, we describe a generic set of Riemannian metrics of the feature space of orientation preference that obeys properties of the shift-twist, translation, and reflection symmetries. Second, these metrics are embedded in a modified Swift-Hohenberg model. As a result we get a pattern formation process that resembles the pattern formation process in the visual cortex. We focus on the final stable patterns that are regular and periodic. In a third step we analyze the influences on pattern formation using weakly nonlinear theory and mode analysis. We compare the results of the present approach with earlier models.     

Evolution of the genetic machinery of the visual cycle: a novelty of the vertebrate eye?

The discovery in invertebrates of ciliary photoreceptor cells and ciliary (c)-opsins established that at least two of the three elements that characterize the vertebrate photoreceptor system were already present before vertebrate evolution. However, the origin of the third element, a series of biochemical reactions known as the "retinoid cycle," remained uncertain. To understand the evolution of the retinoid cycle, I have searched for the genetic machinery of the cycle in invertebrate genomes, with special emphasis on the cephalochordate amphioxus. Amphioxus is closely related to vertebrates, has a fairly prototypical genome, and possesses ciliary photoreceptor cells and c-opsins. Phylogenetic and structural analyses of the amphioxus sequences related with the vertebrate machinery do not support a function of amphioxus proteins in chromophore regeneration but suggest that the genetic machinery of the retinoid cycle arose in vertebrates due to duplications of ancestral nonvisual genes. These results favor the hypothesis that the retinoid cycle machinery was a functional innovation of the primitive vertebrate eye.     

Is there a motion-independent position computation of an object in the visual system of the housefly?

A single vertical stripe (long or short) was moved clockwise, with constant speed, around a tethered femaleMusca domestica fly. The yaw torque response of the fly was analyzed as a function of the position of the object. After an interval of 8 s the stripe was moved counterclockwise and a similar analysis of the torque was made. This procedure was repeated a few times and averaged to each direction separately and for all the flies tested. The results suggested that: a) There are at least two mechanisms for computing the optomotor response in the lower part of the fly's eye, one performing a position-dependent velocity computation and the other depending on the position but not on the direction of motion of an object. b) These two components are parametrized over the position on the lower part of the eye. The results also show that: c) There is a significant difference in the response between the upper and the lower part of the eye. The position-dependent component cannot be detected in the upper part of the eye. In addition: d) Two different control mechanisms are proposed, one responding to progressive (from front to back) and one to regressive (from back to front) movement of objects.     

A fully functional rod visual pigment in a blind mammal. A case for adaptive functional reorganization?

In the blind subterranean mole rat Spalax ehrenbergi superspecies complete ablation of the visual image-forming capability has been accompanied by an expansion of the bilateral projection from the retina to the suprachiasmatic nucleus. We have cloned the open reading frame of a visual pigment from Spalax that shows >90% homology with mammalian rod pigments. Baculovirus expression yields a membrane protein with all functional characteristics of a rod visual pigment (lambda(max) = 497 +/- 2 nm; pK(a) of meta I/meta II equilibrium = 6.5; rapid activation of transducin in the light). We not only provide evidence that this Spalax rod pigment is fully functional in vitro but also show that all requirements for a functional pigment are present in vivo. The physiological consequences of this unexpected finding are discussed. One attractive option is that during adaptation to a subterranean lifestyle, the visual system of this mammal has undergone mosaic reorganization, and the visual pigments have adapted to a function in circadian photoreception.     

Zero-crossing detectors in primary visual cortex?

David Marr and others have hypothesized that the visual system processes complex scene information in stages, the first of which involves the detection of light intensity edges or zero-crossings (Marr, 1982). Ideal zero-crossing detector mechanisms have been described and modeled in terms of their possible physiological implementation (Marr and Hildreth, 1980; Poggio, 1983). We now present evidence of visual cortical receptive fields which resemble in spatial organizational terms the requirements of zero-crossing analysis. The linear and nonlinear summation within and between the receptive field subunits are described and compared with predicted processes. The relative subunit sizes and separations are analyzed in these terms. Our findings support the notion that receptive fields may correspond with zero-crossing filters rather than zero-crossing detector gates.