Neurons encode information in sequences of spikes, which are triggered when their membrane potential crosses a threshold. In vivo, the spiking threshold displays large variability suggesting that threshold dynamics have a profound influence on how the combined input of a neuron is encoded in the spiking. Threshold variability could be explained by adaptation to the membrane potential. However, ...

1. We measured spatial and temporal sensitivity of 81 X-cells and 46 Y-cells in the lateral geniculate nucleus of cats by determining contrast thresholds of single cells to counterphased, sine-wave gratings. The plots of contrast sensitivity (reciprocal of the contrast threshold) as a function of spatial or temporal frequency of the sine-wave grating represent the contrast sensitivity functions...

The lasing threshold of a random laser is computed numerically from a generic model. It is shown that spatial correlations of the disorder in the medium (i.e., dielectric constant) lead to an increase of the decay rates of the eigenmodes and of the lasing threshold. This is in conflict with predictions that such correlations should lower the threshold. While all results are derived for photonic...

Previous work [Vassilev, capital A, Cyrillic., Mihaylova, M., Racheva, K., Zlatkova, M., & Anderson, R. S. (2003). Spatial summation of S-cone ON and OFF signals: Effects of retinal eccentricity. Vision Research, 43, 2875-2884; Vassilev, A., Zlatkova, M., Krumov, A., & Schaumberger, M. (2000). Spatial summation of blue-on yellow light increments and decrements in human vision. Vision Research, ...

To evaluate residual spatial vision deficits in treated amblyopia, we recruited five clinically treated amblyopes (mean age=10.6 years). Contrast sensitivity functions (CSF) in both the previously amblyopic eyes (pAE; visual acuity=0.944+/-0.019 MAR) and fellow eyes (pFE; visual acuity=0.936+/-0.021 MAR) were measured using a standard psychophysical procedure for all the subjects. The results i...