Abstract: The assumption that the retina’s main objective is to provide a minimum entropy representation to higher visual areas (ie efficient coding principle) allows to predict retinal filtering in space–time and colour (Atick, 1992 Network 3 213–251). This is achieved by considering the power spectra of natural images (which is proportional to 1/f2) and the suppression of retinal and image noise. However, most studies consider images within a limited range of lighting conditions (eg near noon) whereas the visual system’s spatial filtering depends on light intensity and the spatiochromatic properties of natural scenes depend of the time of the day. Here, we explore whether the dependence of visual spatial filtering on luminance match the changes in power spectrum of natural scenes at different times of the day. Using human cone-activation based naturalistic stimuli (from the Barcelona Calibrated Images Database), we show that for a range of luminance levels, the shape of the retinal CSF reflects the slope of the power spectrum at low spatial frequencies. Accordingly, the retina implements the filtering which best decorrelates the input signal at every luminance level. This result is in line with the body of work that places efficient coding as a guiding neural principle.

Abstract: In two previous experiments [Parraga et al, 2009 J. of Im. Sci. and Tech 53(3) 031106; Benavente et al,2009 Perception 38 ECVP Supplement, 36] the boundaries of basic colour categories were measured.
In the first experiment, samples were presented in isolation (ie on a dark background) and boundaries were measured using a yes/no paradigm. In the second, subjects adjusted the chromaticity of a sample presented on a random Mondrian background to find the boundary between pairs of adjacent colours.
Results from these experiments showed significant dierences but it was not possible to conclude whether this discrepancy was due to the absence/presence of a colourful background or to the dierences in the paradigms used. In this work, we settle this question by repeating the first experiment (ie samples presented on a dark background) using the second paradigm. A comparison of results shows that
although boundary locations are very similar, boundaries measured in context are significantly dierent(more diuse) than those measured in isolation (confirmed by a Student’s t-test analysis on the subject’s answers statistical distributions). In addition, we completed the mapping of colour name space by measuring the boundaries between chromatic colours and the achromatic centre. With these results we
completed our parametric fuzzy-sets model of colour naming space.

Abstract: JCR Impact Factor 2009: 0.391
In this paper, we present a fuzzy-set of parametric functions which segment the CIE lab space into eleven regions which correspond to the group of common universal categories present in all evolved languages as identified by anthropologists and linguists. The set of functions is intended to model a color-name assignment task by humans and differs from other models in its emphasis on the inter-color boundary regions, which were explicitly measured by means of a psychophysics experiment. In our particular implementation, the CIE lab space was segmented into eleven color categories using a Triple Sigmoid as the fuzzy sets basis, whose parameters are included in this paper. The model’s parameters were adjusted according to the psychophysical results of a yes/no discrimination paradigm where observers had to choose (English) names for isoluminant colors belonging to regions in-between neighboring categories. These colors were presented on a calibrated CRT monitor (14-bit x 3 precision). The experimental results show that inter- color boundary regions are much less defined than expected and color samples other than those near the most representatives are needed to define the position and shape of boundaries between categories. The extended set of model parameters is given as a table.

Abstract: Mirror symmetry is a property most likely to be encountered in animals than in medium scale vegetation or inanimate objects in the natural world. This might be the reason why the human visual system has evolved to detect it quickly and robustly. Indeed, the perception of symmetry assists higher-level visual processing that are crucial for survival such as target recognition and identification irrespective of position and location. Although the task of detecting symmetrical objects seems effortless to us, it is very challenging for computers (to the extent that it has been proposed as a robust “captcha” by Funk & Liu in 2016). Indeed, the exact mechanism of symmetry detection in primates is not well understood: fMRI studies have shown that symmetrical shapes activate specific higher-level areas of the visual cortex (Sasaki et al.; 2005) and similarly, a large body of psychophysical experiments suggest that the symmetry perception is critically influenced by low-level mechanisms (Treder; 2010). In this work we attempt to find plausible low-level mechanisms that might form the basis for symmetry perception. Our simple model is made from banks of (i) odd-symmetric Gabors (resembling edge-detecting V1 neurons); and (ii) banks of larger odd- and even-symmetric Gabors (resembling higher visual cortex neurons), that pool signals from the 'edge image'. As reported previously (Akbarinia et al, ECVP2017), the convolution of the symmetrical lines with the two Gabor kernels of alternative phase produces a minimum in one and a maximum in the other (Osorio; 1996), and the rectification and combination of these signals create lines which hint of mirror symmetry in natural images. We improved the algorithm by combining these signals across several spatial scales. Our preliminary results suggest that such multiscale combination of convolutional operations might form the basis for much of the operation of the HVS in terms of symmetry detection and representation.