scholarly journals The potential roles of saturating and supersaturating contrast-response functions in conjunction detection: Reply to Peirce

2013 ◽  
Vol 13 (4) ◽  
pp. 22-22 ◽  
Author(s):  
K. A. May ◽  
L. Zhaoping
2016 ◽  
Vol 116 (4) ◽  
pp. 1765-1784 ◽  
Author(s):  
Pedro Gabrielle Vieira ◽  
João Paulo Machado de Sousa ◽  
Jerome Baron

The neuronal representation of luminance contrast has not been thoroughly studied in birds. Here we present a detailed quantitative analysis of the contrast response of 120 individual neurons recorded from the visual wulst of awake burrowing owls ( Athene cunicularia). Stimuli were sine-wave gratings presented within the cell classical receptive field and optimized in terms of eye preference, direction of drift, and spatiotemporal frequency. As contrast intensity was increased from zero to near 100%, most cells exhibited a monotonic response profile with a compressive, at times saturating, nonlinearity at higher contrasts. However, contrast response functions were found to have a highly variable shape across cells. With the view to capture a systematic trend in the data, we assessed the performance of four plausible models (linear, power, logarithmic, and hyperbolic ratio) using classical goodness-of-fit measures and more rigorous statistical tools for multimodel inferences based on the Akaike information criterion. From this analysis, we conclude that a high degree of model uncertainty is present in our data, meaning that no single descriptor is able on its own to capture the heterogeneous nature of single-unit contrast responses in the wulst. We further show that the generalizability of the hyperbolic ratio model established, for example, in the primary visual cortex of cats and monkeys is not tenable in the owl wulst mainly because most neurons in this area have a much wider dynamic range that starts at low contrast. The challenge for future research will be to understand the functional implications of these findings.


2019 ◽  
Vol 60 (1) ◽  
pp. 442
Author(s):  
Jia Jia Lek ◽  
Bao N. Nguyen ◽  
Allison M. McKendrick ◽  
Algis J. Vingrys

2006 ◽  
Author(s):  
Zhong-Lin Lu ◽  
Xiangrui Li ◽  
Bosco S. Tjan ◽  
Barbara A. Dosher ◽  
Wilson Chu

Neuroscience ◽  
2008 ◽  
Vol 156 (3) ◽  
pp. 748-757 ◽  
Author(s):  
Y. Yang ◽  
Z. Liang ◽  
G. Li ◽  
Y. Wang ◽  
Y. Zhou ◽  
...  

2005 ◽  
Vol 94 (1) ◽  
pp. 136-146 ◽  
Author(s):  
M. R. Ibbotson

In mammals, many cells in the retino-geniculate-cortical pathway adapt during stimulation with high contrast gratings. In the visual cortex, adaptation to high contrast images reduces sensitivity at low contrasts while only moderately affecting sensitivity at high contrasts, thus generating rightward shifts in the contrast response functions (contrast gain control). Similarly, motion adaptation at particular temporal frequencies (TFs) alters the temporal tuning properties of cortical cells. For the first time in any species, this paper investigates the influence of motion adaptation on both the contrast and TF responses of neurons in the retino-pretectal pathway by recording from direction-selective neurons in the nucleus of the optic tract (NOT) of the marsupial wallaby, Macropus eugenii. This species is of interest because its NOT receives almost all input directly from the retina, with virtually none from the visual cortex (unlike cats and primates). All NOT cells show changes in their contrast response functions after adaptation, many revealing contrast gain control. Contrast adaptation is direction-dependent, preferred directions producing the largest changes. The lack of cortical input suggests that contrast adaptation is generated independently from the cortex in the NOT or retina. Motion adaptation also produces direction-selective effects on the TF tuning of NOT neurons by shifting the location of the optimum TF. Cells that show strong adaptation to contrast also tend to show large changes in TF tuning, suggesting similar intracellular mechanisms. The data are discussed in terms of the generality of contrast adaptation across mammalian species and across unconnected brain regions within the same species.


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