Simulation of Cortex Visual Cells for Texture Segmentation: Foveal and Parafoveal Projections

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 120-120
Author(s):  
P M Palagi ◽  
A Guérin-Dugué

The objective of this work is to simulate visual cortical cells, their sensitivities to frequencies and orientations, and their part in texture segmentation. The simulation of these cells is realised through band-pass, oriented filters (Gabor filters), and multiresolution image decomposition. By this means, the filter sensitivities represent cell sensitivities to preferred orientations according to their frequency and orientation bandwidths, and multiresolution represents the different band frequencies. For texture analysis and segmentation, overlaying of band-pass filters is necessary to completely cover the Fourier domain. A continuous sensitivity to frequency and orientation is achieved by the filters overlapping and consequently by their interpolation. We used here four octave frequency bands from 1 to 16 cycles deg−1 and six orientations per band. The results obtained for texture segmentation with these parameters are very promising (up to 97% recognition rate) [Guérin-Dugué and Palagi, 1994 Neural Processing Letters1(1) 25 – 29]. The images analysed cover a multitude of different domains such as psychophysical tests and natural textures of different roughness. In order to create a cortical cell representation closer to neurophysiological data, and to improve texture segmentation results, we represent cell sensitivities by their foveal and parafoveal projections [R L DeValois, K K DeValois, 1988 Spatial Vision (Oxford: Oxford Science Publications)]. Cells receiving projections from the foveal zone are modeled by five octave frequency bands (from 0.5 to 16 cycles deg−1) and six orientations. Cells receiving projections from the parafoveal zone have the same sensitivities but are modeled by four octave frequency bands (from 0.5 to 8 cycles deg−1). By using these two different resolutions, preliminary tests have shown the capability of detecting textured regions by the parafoveal projection and localisation of boundaries by the foveal projection.

1984 ◽  
Vol 51 (3) ◽  
pp. 481-499 ◽  
Author(s):  
S. Reinis ◽  
J. P. Landolt ◽  
D. S. Weiss ◽  
K. E. Money

/he spontaneous and evoked unit activities of complex visual cortical cells were recorded from Brodmann's area 18 in immobilized, unanesthetized cats before, during, and after stimulation of the vestibular system. The vestibular system was stimulated by intravenous injection of deuterium oxide (D2O)--a noted nystagmogenic agent (14)--or by direct galvanic stimulation of the labyrinth. Measures of the receptive-field areas, poststimulus time histograms, directional preferences, and the optimal speed of the light bar stimulating the cell were obtained before and after the application of D2O. Directional preferences were determined in a novel manner, using a method derived from a hierarchical clustering technique (19). Data were collected and analyzed from a) visual cortical cells in cats with intact labyrinths, b) visual cortical cells in cats following bilateral labrinthectomies, and c) nonvisual cortical cells in cats with intact labyrinths. In cats with intact labyrinths, D2O changed the optimal length of the light bar that was able to stimulate the cortical cell as well as the path on which it evoked the response of the cell. Both values, which constitute the receptive field of the cell, changed approximately proportionately. This effect usually lasts for less than 4.5 h. The other cellular characteristics were also altered by the D2O. Galvanic stimulation of the labyrinth resembles, in its effects, the injection of D2O. In labyrinth-intact cats, the time course of area 18 spontaneous activity dramatically increased 30 min or more after D2O was administered. It peaked 2-3 h later and still had not returned to preinjection levels even 7 h after the D2O administration. In bilaterally labyrinthectomized cats, the spontaneous activity of the visual cells (and the other cellular characteristics studied) did not change following D2O administration. In nonvisual cells from labyrinth-intact cats, the spontaneous activity demonstrated a slight but significant decrease over time after D2O injection. (The other measures, however, did not change.) In pilot studies (about 2 wk prior to the electrophysiological experiments), the cats were injected with D2O. Within 8-10 min afterward, signs of positional nystagmus commenced; and within 30 min, problems in maintaining balance were noted. This continued for 7-8 h before disappearing. In the labyrinthectomized animals, such effects were not observed. These results, therefore, add support to other evidence that suggests that D2O works directly through the vestibular apparatus to produce the effects it does (and not through interference with certain cellular processes).(ABSTRACT TRUNCATED AT 400 WORDS)


2000 ◽  
Vol 522 (1) ◽  
pp. 59-76 ◽  
Author(s):  
Maxim Volgushev ◽  
Trichur R. Vidyasagar ◽  
Marina Chistiakova ◽  
Tagrid Yousef ◽  
Ulf T. Eysel

1999 ◽  
Vol 11 (1) ◽  
pp. 21-66 ◽  
Author(s):  
Douglas A. Miller ◽  
Steven W. Zucker

We present a model of visual computation based on tightly inter-connected cliques of pyramidal cells. It leads to a formal theory of cell assemblies, a specific relationship between correlated firing patterns and abstract functionality, and a direct calculation relating estimates of cortical cell counts to orientation hyperacuity. Our network architecture is unique in that (1) it supports a mode of computation that is both reliable and efficent; (2) the current-spike relations are modeled as an analog dynamical system in which the requisite computations can take place on the time scale required for an early stage of visual processing; and (3) the dynamics are triggered by the spatiotemporal response of cortical cells. This final point could explain why moving stimuli improve vernier sensitivity.


10.1038/73957 ◽  
2000 ◽  
Vol 3 (4) ◽  
pp. 384-390 ◽  
Author(s):  
Matthew T. Schmolesky ◽  
Youngchang Wang ◽  
Mingliang Pu ◽  
Audie G. Leventhal

1968 ◽  
Vol 198 (1) ◽  
pp. 237-250 ◽  
Author(s):  
F. W. Campbell ◽  
B. G. Cleland ◽  
G. F. Cooper ◽  
Christina Enroth-Cugell

1972 ◽  
Vol 2 (2) ◽  
pp. 135-143 ◽  
Author(s):  
G. A. Borger ◽  
T. T. Kozlowski

The subepidermal cell layer was the site of origin of the first periderm in the hypocotyl and internodes of Fraxinuspennsylvanica and Ailanthusaltissima. In the hypocotyl of Robiniapsendoacacia, the first periderm arose in cortical cells near the phloem; in the internodes it originated in the subepidermal, second, or third cortical cell layer. The outermost cell layer of the pericycle gave rise to the first periderm in the hypocotyl of Pinusresinosa. In all four species, periderm appeared first near the base of the hypocotyl and developed acropetally. In A. altissima and R. pseudoaeacia, phellem mother cells were cut off by the phellogen. These subsequently divided to produce phellem cells. In F. pennsylvanica and P. resinosa, phellem cells were produced directly from the phellogen.


Sign in / Sign up

Export Citation Format

Share Document