Spatial and Temporal Frequency Tuning of Motion-in-Depth Aftereffect

2008 ◽  
Vol 128 (7) ◽  
pp. 1015-1022
Author(s):  
Sheng Ge ◽  
Makoto Ichikawa ◽  
Atsushi Osa ◽  
Keiji Iramina ◽  
Hidetoshi Miike
2008 ◽  
Vol 25 (7) ◽  
pp. 1574 ◽  
Author(s):  
Satoshi Shioiri ◽  
Tomohiko Nakajima ◽  
Daisuke Kakehi ◽  
Hirohisa Yaguchi

2010 ◽  
Vol 5 (1) ◽  
pp. 21-30 ◽  
Author(s):  
Alice Rokszin ◽  
Zita Márkus ◽  
Gábor Braunitzer ◽  
Antal Berényi ◽  
Marek Wypych ◽  
...  

AbstractOur study compares the spatio-temporal visual receptive field properties of different subcortical stages of the ascending tectofugal visual system. Extracellular single-cell recordings were performed in the superficial (SCs) and intermediate (SCi) layers of the superior colliculus (SC), the suprageniculate nucleus (Sg) of the posterior thalamus and the caudate nucleus (CN) of halothane-anesthetized cats. Neuronal responses to drifting gratings of various spatial and temporal frequencies were recorded. The neurons of each structure responded optimally to low spatial and high temporal frequencies and displayed narrow spatial and temporal frequency tuning. The detailed statistical analysis revealed that according to its stimulus preferences the SCs has markedly different spatio-temporal properties from the homogeneous group formed by the SCi, Sg and CN. The SCs neurons preferred higher spatial and lower temporal frequencies and had broader spatial tuning than the other structures. In contrast to the SCs the visually active SCi, as well as the Sg and the CN neurons possessed consequently similar spatio-temporal preferences. These data support our hypothesis that the visually active SCi, Sg and CN neurons form a homogeneous neuronal population given a similar spatio-temporal frequency preference and a common function in processing of dynamic visual information.


1997 ◽  
Vol 14 (4) ◽  
pp. 741-749 ◽  
Author(s):  
Colin W.G. Clifford ◽  
Michael R. Ibbotson ◽  
Keith Langley

AbstractThere are marked similarities in the adaptation to motion observed in wide-field directional neurons found in the mammalian nucleus of the optic tract and cells in the insect lobula plate. However, while the form and time scale of adaptation is comparable in the two systems, there is a difference in the directional properties of the effect. A model based on the Reichardt detector is proposed to describe adaptation in mammals and insects, with only minor modifications required to account for the differences in directionality. Temporal-frequency response functions of the neurons and the model are shifted laterally and compressed by motion adaptation. The lateral shift enhances dynamic range and differential motion sensitivity. The compression is not caused by fatigue, but is an intrinsic property of the adaptive process resulting from interdependence of temporal-frequency tuning and gain in the temporal filters of the motion detectors.


Some computational theories of motion perception assume that the first stage en route to this perception is the local estimate of image velocity. However, this assumption is not supported by data from the primary visual cortex. Its motion sensitive cells are not selective to velocity, but rather are directionally selective and tuned to spatio-temporal frequen­cies. Accordingly, physiologically based theories start with filters selec­tive to oriented spatio-temporal frequencies. This paper shows that computational and physiological theories do not necessarily conflict, because such filters may, as a population, compute velocity locally. To prove this point, we show how to combine the outputs of a class of frequency tuned filters to detect local image velocity. Furthermore, we show that the combination of filters may simulate ‘Pattern’ cells in the middle temporal area (MT), whereas each filter simulates primary visual cortex cells. These simulations include three properties of the primary cortex. First, the spatio-temporal frequency tuning curves of the in­dividual filters display approximate space-time separability. Secondly, their direction-of-motion tuning curves depend on the distribution of orientations of the components of the Fourier decomposition and speed of the stimulus. Thirdly, the filters show facilitation and suppression for responses to apparent motions in the preferred and null directions, respect­ively. It is suggested that the MT’s role is not to solve the aperture problem, but to estimate velocities from primary cortex information. The spatial integration that accounts for motion coherence may be postponed to a later cortical stage.


2010 ◽  
Vol 31 (6) ◽  
pp. 1043-1062 ◽  
Author(s):  
Hsin-Hao Yu ◽  
Richa Verma ◽  
Yin Yang ◽  
Heath A. Tibballs ◽  
Leo L. Lui ◽  
...  

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 12-12
Author(s):  
P J Bex ◽  
F A J Verstraten ◽  
I Mareschal

The motion aftereffect (MAE) was used to study the temporal-frequency and spatial-frequency selectivity of the visual system at suprathreshold contrasts. Observers adapted to drifting sine-wave gratings of a range of spatial and temporal frequencies. The magnitude of the MAE induced by the adaptation was measured with counterphasing test gratings of a variety of spatial and temporal frequencies. Independently of the spatial or temporal frequency of the adapting grating, the largest MAE was found with slowly counterphasing test gratings (∼0.125 – 0.25 Hz). For slowly counterphasing test gratings (<∼2 Hz), the largest MAEs were found when the test grating was of similar spatial frequency to that of the adapting grating, even at very low spatial frequencies (0.125 cycle deg−1). However, such narrow spatial frequency tuning was lost when the temporal frequency of the test grating was increased. The data suggest that MAEs are dominated by a single, low-pass temporal-frequency mechanism and by a series of band-pass spatial-frequency mechanisms at low temporal frequencies. At higher test temporal frequencies, the loss of spatial-frequency tuning implicates separate mechanisms with broader spatial frequency tuning.


2020 ◽  
Vol 14 ◽  
Author(s):  
Daniela Camillo ◽  
Mehran Ahmadlou ◽  
J. Alexander Heimel

1996 ◽  
Vol 716 (1-2) ◽  
pp. 219-223 ◽  
Author(s):  
Eric Tardif ◽  
André Bergeron ◽  
Franco Lepore ◽  
Jean-Paul Guillemot

2005 ◽  
Vol 94 (2) ◽  
pp. 1645-1650 ◽  
Author(s):  
Baowang Li ◽  
Matthew R. Peterson ◽  
Jeffrey K. Thompson ◽  
Thang Duong ◽  
Ralph D. Freeman

The response of a cell in the primary visual cortex to an optimally oriented grating is suppressed by a superimposed orthogonal grating. This cross-orientation suppression (COS) is exhibited when the orthogonal and optimal stimuli are presented to the same eye (monoptically) or to different eyes (dichoptically). A recent study suggested that monoptic COS arises from subcortical processes; however, the mechanisms underlying dichoptic COS were not addressed. We have compared the temporal frequency tuning and stimulus adaptation properties of monoptic and dichoptic COS. We found that dichoptic COS is best elicited with lower temporal frequencies and is substantially reduced after prolonged adaptation to a mask grating. In contrast, monoptic COS is more pronounced with mask gratings at much higher temporal frequencies and is less prone to stimulus adaptation. These results suggest that monoptic COS is mediated by subcortical mechanisms, whereas intracortical inhibition is the mechanism for dichoptic COS.


2016 ◽  
Vol 16 (12) ◽  
pp. 1217 ◽  
Author(s):  
Shui'Er Han ◽  
Claudia Lunghi ◽  
David Alais

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