The concept of working memory is key to cognitive functioning. Working memory encompasses the capacity to retain immediately past information, to process this information, and to use it to guide goal-directed behavior. Corvid songbirds are renowned for their high-level cognitive capabilities, but where and how visual information is temporarily retained by neurons in the avian brain in a behaviorally relevant way remains poorly understood. We trained four carrion crows (Corvus corone) on versions of a delayed match-to-sample task that required the crows to remember a visual stimulus for later comparison. While the crows performed the task, we recorded the activity of single neurons in the nidopallium caudolaterale (NCL), a pallial association area of the avian endbrain. We show that many NCL neurons encode information about visual stimuli and temporarily maintain this information after the stimulus disappeared by sustained delay activity. Selective delay activity allows the birds to hold relevant information in memory and correlates with discrimination behavior. This suggests that sustained activity of NCL neurons is a neuronal correlate of visual working memory in the corvid brain and serves to bridge temporal gaps, thereby offering a workspace for processing immediately past visual information.
Evolutionary, cognitive, and neural underpinnings of mammalian play are not yet fully elucidated. We played hide-and-seek, an elaborate role-play game, with rats. We did not offer food rewards but engaged in playful interactions after finding or being found. Rats quickly learned the game and learned to alternate between hiding versus seeking roles. They guided seeking by vision and memories of past hiding locations and emitted game event–specific vocalizations. When hiding, rats vocalized infrequently and they preferred opaque over transparent hiding enclosures, a preference not observed during seeking. Neuronal recordings revealed intense prefrontal cortex activity that varied with game events and trial types (“hide” versus “seek”) and might instruct role play. The elaborate cognitive capacities for hide-and-seek in rats suggest that this game might be evolutionarily old.
Can the adult brain assimilate a novel, topographically organized, sensory modality into its perceptual repertoire? To test this, we implemented a microstimulation-based neuroprosthesis that rats used to discriminate among infrared (IR) light sources. This system continuously relayed information from four IR sensors that were distributed to provide a panoramic view of IR sources, into primary somatosensory cortex (S1). Rats learned to discriminate the location of IR sources in Ͻ4 d. Animals in which IR information was delivered in spatial register with whisker topography learned the task more quickly. Further, in animals that had learned to use the prosthesis, altering the topographic mapping from IR sensor to stimulating electrode had immediate deleterious effects on discrimination performance. Multielectrode recordings revealed that S1 neurons had multimodal (tactile/IR) receptive fields, with clear preferences for those stimuli most likely to be delivered during the task. Neuronal populations predicted, with high accuracy, which stimulation pattern was present in small (75 ms) time windows. Surprisingly, when identical microstimulation patterns were delivered during an unrelated task, cortical activity in S1 was strongly suppressed. Overall, these results show that the adult mammalian neocortex can readily absorb completely new information sources into its representational repertoire, and use this information in the production of adaptive behaviors.
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