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H S Orbach

Publications and source records attributed to H S Orbach.

8 recordsLinked to original sources
PubMed2001

Anisotropy in judging the absolute direction of motion.

The angular dependence of precision measurements is well established as the oblique effect in motion perception. Recently, it has been shown that the visual system also exhibits anisotropic behaviour with respect to accuracy of the absolute direction of motion of random dot fields. This study aimed to investigate whether this angular dependent, directional bias is a general phenomenon of motion perception. Our results demonstrate, for single translating tilted lines viewed foveally, an extraordinary illusion with perceptual deviations of up to 35 degrees from veridical. Not only is the magnitude of these deviations substantially larger than that for random dots, but the general pattern of the illusion is also different from that found for dot fields. Significant differences in the bias, as a function of line tilt and line length, suggest that the illusion does not result from fixed inaccuracies of the visual system in the computation of direction of motion. Potential sources for these large biases are motion integration mechanisms. These were also found to be anisotropic. The anisotropic nature and the surprisingly large magnitude of the effect make it a necessary consideration in analyses of motion experiments and in modelling studies.

Anisotropy↗
PubMed1999

Computing feature motion without feature detectors: a model for terminator motion without end-stopped cells.

Pointlike object features such as line-endings, have a privileged position in the computation of the veridical direction of object motion. Experiments confirm that the human visual system relies heavily on such features if they are present. It has been proposed that units such as end-stopped cells might be necessary for the computation of feature motion instead of the simple cells used in plaid motion models. Conventional plaid motion models have not been applied to feature motion. We present here a model, based on ordinary simple cells, using two parallel pathways (Fourier and non-Fourier) for the computation of the direction of two dimensional motion. Although similar in structure to popular models of plaid motion, our model includes a novel scheme for contrast normalisation and incorporates spatial pooling at the level of MT cells. The model predictions are consistent with psychophysical results for plaids. Furthermore, it computes directions within 5 degrees of the physical motion of line-endings. It is shown that the non-Fourier signal is necessary for the computation of veridical motion.

Computer Simulation↗
PubMed1999

Factors limiting peripheral pattern discrimination.

Previous reports indicate that some foveally discriminable compound gratings are indiscriminable in peripheral vision, even when they are scaled by the ratio of peripheral to foveal grating acuity. To determine the stimulus properties that limit peripheral discrimination, we used Gaussian derivatives of various orders. These patterns are spatially localized and have intrinsic even or odd symmetry. Our results show that certain odd symmetric patterns are discriminable in the periphery, while others are not. Furthermore, certain even symmetric patterns are not peripherally discriminable. These data are consistent with three limitations on peripheral pattern discrimination: (1) Patterns that produce different maximum neural responses will be peripherally discriminable. (2) Positional uncertainty and undersampling degrade discrimination of high spatial frequency patterns in the periphery. (3) Patterns generating substantial neural activity within a constrained region are processed as textures in peripheral vision so that pattern details within that region are no longer available for discrimination. A neural model incorporating inhibition of simple cells by complex cells implements a transition between contour analysis and texture analysis in peripheral vision and explains the experimental data.

Fovea Centralis↗
PubMed1998

Contrast discrimination, non-uniform patterns and change blindness.

Change blindness--our inability to detect large changes in natural scenes when saccades, blinks and other transients interrupt visual input--seems to contradict psychophysical evidence for our exquisite sensitivity to contrast changes. Can the type of effects described as 'change blindness' be observed with simple, multi-element stimuli, amenable to psychophysical analysis? Such stimuli, composed of five mixed contrast elements, elicited a striking increase in contrast increment thresholds compared to those for an isolated element. Cue presentation prior to the stimulus substantially reduced thresholds, as for change blindness with natural scenes. On one hand, explanations for change blindness based on abstract and sketchy representations in short-term visual memory seem inappropriate for this low-level image property of contrast where there is ample evidence for exquisite performance on memory tasks. On the other hand, the highly increased thresholds for mixed contrast elements, and the decreased thresholds when a cue is present, argue against any simple early attentional or sensory explanation for change blindness. Thus, psychophysical results for very simple patterns cannot straightforwardly predict results even for the slightly more complicated patterns studied here.

Adult↗
PubMed1993

In vivo tracing of pathways and spatio-temporal activity patterns in rat visual cortex using voltage sensitive dyes.

We monitored optical signals from cortex stained with a voltage sensitive dye to study activity evoked by intracortical electrical stimulation. The objectives were to study the spatial and temporal spread of activity from intrinsic connections near the stimulating electrode and to develop a new technique to study extrinsic projections from striate cortex to extrastriate target areas. Various measures were made of the time course of the optical signal (latency, rise time, decay time, temporal summation, facilitation versus depression, and presence or absence of a slow undershoot); in general, these measures were found to vary significantly across different response positions, different experiments, and even different runs within the same experiment. The spatial distribution of responses near the stimulating electrode in striate cortex was usually elliptical and was most often elongated along the anterior-posterior axis, with a typical size (full width at 75% max) of 1.3 mm (anterior-posterior axis) by 0.75 mm (medio-lateral axis). In some cases, complex spatio-temporal patterns were observed, in which the position of the maximum optical signal shifted with time or split into multiple peaks. In eight experiments, a response focus was found in extrastriate cortex at an expected location within the lateromedial area (LM). The response focus in LM was typically about half the size of that in striate cortex. In some experiments we observed additional focal responses in the anterolateral visual area (AL). The extrastriate responses showed a significant delay (3-10 ms) in onset and time to peak relative to the striate response. The validity of this technique for determining extrinsic projections was tested in two types of experiments. In the first, stimulation from two electrodes in striate cortex generated response foci consistent with the known topographic organization of area LM. In the second, the optically measured response focus was shown to correlate with the histologically reconstructed projection of a chemical tracer injected near the site of stimulation. We discuss the chain of neurophysiological events that occur during and after focal electrical stimulation and how they relate to the observed optical signal. We conclude that direct passive responses were a small component of our signal, that the component due to action potentials in directly stimulated neurons should have occurred in the first 1-2 ms post stimulus and is small compared to the peak signal, and that overall our signals were probably dominated by a combination of asynchronously occurring action potentials and excitatory and inhibitory synaptic potentials.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1985

Optical mapping of electrical activity in rat somatosensory and visual cortex.

We have investigated the use of optical methods for monitoring neuron activity in mammalian cortex. The cortex was stained with a voltage-sensitive dye and fluorescence was simultaneously measured from 124 areas using a photodiode array. Optical signals were detected in rat somatosensory cortex in response to small whisker movements and in visual cortex in response to light flashes to the eye. Relatively large signals were obtained during focal interictal epileptiform discharges induced by bicuculline. The measuring system had a time resolution of milliseconds and a spatial resolution of a few hundred micrometers. Simultaneous, multi-site optical recordings of activity may provide a new and potentially powerful method for studying function and dysfunction in mammalian cortex.

Animals↗
PubMed1983

Optical monitoring of activity from many areas of the in vitro and in vivo salamander olfactory bulb: a new method for studying functional organization in the vertebrate central nervous system.

We have investigated the use of voltage-sensitive dyes to monitor neuronal activity in the intact salamander olfactory bulb. After a 10- to 20-min staining period, a magnified image of an in vitro or an in vivo preparation was formed on a 124-element photodiode array. The array was used to simultaneously record absorption or fluorescence changes from 124 adjacent areas of the bulb. At the magnifications used, each detector received light from 100 to 1000 neurons. Relatively large absorption and fluorescence signals were found in response to olfactory nerve stimulation; all of the results presented were from single trials. Because of the large signal size, measurements on in vivo preparations using epi-illumination also had good signal-to-noise ratios. There were significant differences in signal time course between adjacent detectors which suggested a spatial resolution on the order of 200 microns. Tentative assignments of the cellular origins of some signals could be made from the results of paired volley experiments. The results suggest that optical monitoring of membrane potential could provide a useful method for studying neuronal organization in the intact vertebrate central nervous system.

Ambystoma↗