Touchscreen setups are increasingly used in rodents for a wide range of cognitive tasks, including visual discrimination. The greater automation and high throughput of this platform could greatly facilitate future vision research. However, little information is available regarding decision distance and on the limitations of stimulus size. Especially when studying visual functions, the lack of control of basic visual properties is a drawback. Therefore, we determined the maximal number of cycles per screen gratings can have so that Long Evans rats can reliably perform orientation discrimination. To relate our results to literature on visual acuity we tried to make an estimate of the decision distance in the touchscreen platform. The rats can discriminate between orientations with 70% accuracy up to 44 cycles per screen. This could roughly translates to the previously reported visual acuity of 1 c/degree assuming a viewing distance of 12.5 cm. This could be useful when designing new stimuli based on published results in c/degree. One could assume a viewing distance of 12.5 cm and expect similar discrimination performance in the touchscreen setup as in other tasks with a predefined viewing distance.

The images projected onto the retina can vary widely for a single object. Despite these transformations primates can quickly and reliably recognize objects. At the neural level, transformation tolerance in monkey inferotemporal cortex is affected by the temporal contiguity statistics of the visual input. Here we investigated whether temporal contiguity learning also influences the basic feature detectors in lower levels of the visual hierarchy, in particular the independent coding of orientation and spatial frequency (SF) in primary visual cortex. Eight male Long Evans rats were repeatedly exposed to a temporal transition between two gratings that changed in SF and had either the same (control SF) or a different (swap SF) orientation. Electrophysiological evidence showed that the responses of single neurons during this exposure were sensitive to the change in orientation. Nevertheless, the tolerance of orientation selectivity for changes in SF was unaffected by the temporal contiguity manipulation, as observed in 239 single neurons isolated pre-exposure and 234 post-exposure. Temporal contiguity learning did not affect orientation selectivity in V1. The basic filter mechanisms that characterize V1 processing seem unaffected by temporal contiguity manipulations.