Predation without direction selectivity.

Across the animal kingdom, visual predation relies on motion-sensing neurons in the superior colliculus (SC) and its orthologs. These neurons exhibit complex stimulus preferences, including direction selectivity, which is thought to be critical for tracking the unpredictable escape routes of prey. The source of direction selectivity in the SC is contested, and its contributions to predation have not been tested experimentally. Here, we use type-specific cell removal to show that narrow-field (NF) neurons in the mouse SC guide predation. In vivo recordings demonstrate that direction-selective responses of NF cells are independent of recently reported stimulus-edge effects. Monosynaptic retrograde tracing reveals that NF cells receive synaptic input from direction-selective ganglion cells. When we eliminate direction selectivity in the retina of adult mice, direction-selective responses in the SC, including in NF cells, are lost. However, eliminating retinal direction selectivity does not affect the hunting success or strategies of mice, even when direction selectivity is removed after mice have learned to hunt, and despite abolishing the gaze-stabilizing optokinetic reflex. Thus, our results identify the retinal source of direction selectivity in the SC. They show that NF cells in the SC guide predation, an essential spatial orienting task, independent of their direction selectivity, revealing behavioral multiplexing of complex neural feature preferences and highlighting the importance of feature-selective manipulations for neuroethology.

Vision: Rules of thalamic mixology.

The retina generates rich feature representations of the visual world that pass through the thalamus on their way to cortex and perception. A new study reveals rules that govern the separation and combination of retinal inputs in the thalamus.

What psychological process is reflected in the FN400 event-related potential component?

During many recognition contexts, old items elicit a more positive event-related potentials (ERPs) than new items at mid-frontal electrodes about 300-500ms. The psychological processes that are reflected in is ERP component (i.e., the FN400) has been vigorously debated. Some argue that the FN400 reflects familiarity, whereas others argue that it reflects conceptual implicit memory. Three experiments contrasted these two hypotheses by presenting pre-experimentally familiar (i.e., name-brand) products and novel, off-brand products. In addition, some of the off-brand products were conceptually primed by the name-brand product to determine how FN400 amplitude would be affected by conceptually primed, but novel, products. The results provided mixed support for both theoretical views, and it is integrated with a broader theoretical framework to characterize the psychological processes captured by the FN400.