Biomedical subjects

V P Ferrera

Publications and source records attributed to V P Ferrera.

8 recordsLinked to original sources

PubMed1995

Attention and target selection for smooth pursuit eye movements.

Two rhesus monkeys were trained to track a small moving target in the presence of a moving distractor. The target and distractor were distinguished by their color. Smooth pursuit eye movements were quantified in terms of the latency of the eye movement and the open-loop eye acceleration profile. Smooth pursuit latencies for single targets were on the order of 100 msec. When the target was paired with a distractor moving in the same direction as the target, pursuit latencies decreased to roughly 85 msec. When the target was paired with a distractor moving in the opposite direction, pursuit latencies increased to roughly 150 msec. The motion of the distractor had no significant effect on the eye acceleration profile. Experiments were performed to dissociate visual search for the target from pursuit initiation by providing a spatial cue rather than the color cue. These experiments showed that visual search necessarily preceded pursuit initiation only when the distractor moved in the opposite direction relative to the target. In this case, visual search contributed about 25 msec to the overall latency of pursuit. Control experiments showed that the monkey need not attend to the distractor in order for it to influence the latency of pursuit. A network model was developed in which units that represent the motions of the target and distractor compete against one another. Attention serves to bias the outcome of this competition toward the direction of the selected target. The performance of this network exhibits a striking parallel to the effect of the distractor on smooth pursuit latency.

Animals↗

PubMed1992

Mixed parvocellular and magnocellular geniculate signals in visual area V4.

Visual information from the retina is transmitted to the cerebral cortex by way of the lateral geniculate nucleus (LGN) in the thalamus. In primates, most of the retinal ganglion cells that project to the LGN belong to one of two classes, P and M, whose axons terminate in the parvocellular or magnocellular subdivisions of the LGN. These cell classes give rise to two channels that have been distinguished anatomically, physiologically and behaviourally. The visual cortex also can be subdivided into two pathways, one specialized for motion processing and the other for colour and form information. Several lines of indirect evidence have suggested a close correspondence between the subcortical and cortical pathways, such that the M channel provides input to the motion pathway and the P channel drives the colour/form pathway. This hypothesis was tested directly by selectively inactivating either the magnocellular or parvocellular subdivision of the LGN and recording the effects on visual responses in the cortex. We have previously reported that, in accordance with the hypothesis, responses in the motion pathway in the cortex depend primarily on magnocellular LGN. We now report that in the colour/form pathway, visual responses depend on both P and M input. These results argue against a simple correspondence between the subcortical and cortical pathways.

Animals↗

PubMed1992

A psychophysically motivated model for two-dimensional motion perception.

A quantitative model is developed to predict the perceived direction of moving two-dimensional patterns. The model incorporates both a simple motion energy pathway and a "texture boundary motion" pathway that incorporates response squaring before the extraction of motion energy. These pathways correspond to Fourier and non-Fourier motion pathways and are hypothesized to reflect processing in the V1-MT and V1-V2-MT pathway, respectively. A cosine-weighted sum of these pathways followed by competitive feedback inhibition accurately predicts the perceived direction for patterns composed of two cosine gratings at different orientations ("plaids"). The model also predicts direction discrimination, differences between foveal and peripheral viewing, changes in perceived direction with exposure duration, motion masking, and motion transparency.

Computer Simulation↗

PubMed1991

Perceived speed of moving two-dimensional patterns.

When two cosine gratings drifting in different directions are superimposed they can form a coherently moving two-dimensional pattern (plaid) whose resultant speed is related to the component velocities by a geometric construction known as the intersection-of-constraints (IOC). When measured against a standard which has the same spatial frequency as its components, a plaid always appears to move slower than the IOC prediction. However, the perceived speed is generally faster than would be predicted if speed were judged based on the temporal frequency of either the components or the nodes of the plaid. On the other hand, when the standard has the same spatial period as the nodes, the plaid appears to move at the same rate as the predicted IOC resultant. Furthermore, a grating with the same spatial period as the nodes appears to move slower than a grating at the component spatial frequency, just the plaid does. It is therefore likely that speed is encoded similarly for both gratings and plaids, and that the perceived speed of both is determined by the spatial periodicity of the pattern. We have previously classified 2D moving patterns as either type I (resultant lies between component directions) or type II (resultant outside of components). We find that the perceived speed of both types can be accounted for on the basis of the nodal spatial period. Finally we present a model for velocity coding which is based on the responses of spatio-temporal mechanisms.

Contrast Sensitivity↗

PubMed1990

Perceived direction of moving two-dimensional patterns.

When two drifting cosine gratings are superimposed, they will, under appropriate conditions, form a coherently moving two-dimensional pattern whose resultant direction of motion may either be between (type I), or outside (type II) the directions of the two components. We have previously shown that type I patterns produce much stronger masking than either of their components, while type II patterns do not. In this study, we measured perceived direction of motion and thresholds for discrimination of motion direction. We found that type II patterns had a perceived bias of about 7.5 deg toward the direction of their components, and had discrimination thresholds around 6.5 deg, whereas type I patterns had discrimination thresholds around 1.0 deg and no significant bias. We conclude that the neural mechanisms which compute two-dimensional image motion do not strictly implement the intersection-of-constraints construction proposed by Adelson and Movshon (1982).

Discrimination, Psychological↗

PubMed1988

Spatial frequency and orientation tuning of spatial visual mechanisms in human albinos.

A masking paradigm was used to measure the spatial frequency and orientation tuning of spatial mechanisms in the albino visual system. Threshold elevation curves obtained in this manner at test spatial frequencies of 0.25 cycles/deg (cpd), 0.50 cpd, and 1 cpd have the same shape as curves obtained from normal subjects at test frequencies two octaves higher. Additional masking studies showed that contrast processing in albinos obeys the same compressive power law as in normals. Thus, spatial mechanisms in albino central vision have normal spatial frequency and orientation bandwidths. As central cones in the albino are spaced 3-4 times further apart than in the normal fovea, these results support the hypothesis that monocular spatial vision in albinos is primarily limited by this increased receptor spacing. It is hypothesized that this, in turn, is the result of arrested development of the albino retina.

Adult↗

PubMed1987

Direction specific masking and the analysis of motion in two dimensions.

We measured the effects of moving two-component cosine grating masks on the detectability of a moving spatially localized test pattern with a 1.0 octave spatial frequency bandwidth. Masking was used to distinguish between two-component patterns with fluid motion (blobs) and those with rigid motion (plaids). The two gratings which made up the two-dimensional masking patterns were always of the same spatial frequency and contrast, but moved in different directions. We find that plaid masks consistently produced threshold elevations that are 2.0-4.0 times greater than are produced by a single component mask at twice the contrast. Furthermore, this effect is nearly independent of the angle between the two mask components. For fluid motion, however, masking is determined by the mask component whose direction of motion is closest to that of the test. The results obtained with moving two-dimensional patterns demonstrate that, for blobs, the motion of the pattern as a whole has no effect on the degree of masking, whereas, for plaids, the signals arising from the two components interact in a nonlinear manner, thus producing a substantial enhancement of masking, which is clearly related to the coherent motion of the entire pattern. These data shed light on the properties of higher order motion units (possibly in MT cortex) that respond to the direction of two-dimensional pattern motion, suggesting that they combine, in a nonlinear manner, the outputs of units which respond independently to the direction of each mask component.

Form Perception↗

PubMed1985

Spatial frequency tuning of transient non-oriented units.

Thresholds for a vertical test stimulus with a 1.0 octave bandwidth were measured as a function of the spatial frequency of a horizontal flickering cosine mask. Both test and mask were temporally modulated at 8.0 Hz, as low temporal frequencies were found to produce very little masking. Separate experiments were run at each of 10 test frequencies from 0.25 to 8.0 cycles per degree (c/deg) at 0.5 octave intervals. Masking curves thus obtained for each of three subjects were used to compute the spatial frequency sensitivities of three non-oriented mechanisms. Compared to previous masking studies of orientation selective units, non-oriented units have somewhat broader spatial frequency sensitivity curves, in agreement with primate neurophysiology.

Form Perception↗