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Abstract Although macaques and marmosets are both primates of choice for studying the brain mechanisms of cognition, they differ in key aspects of anatomy and behavior. Interestingly, recent connectomic analysis revealed that strong top-down projections from the prefrontal cortex to the posterior parietal cortex, present in macaques and important for executive function, are absent in marmosets. Here, we propose a consensus mapping that bridges the two species’ cortical atlases and allows for direct area-to-area comparison of their connectomes, which are then used to build comparative computational large-scale modeling of the frontoparietal circuit for working memory. We found that the macaque model exhibits resilience against distractors, a prerequisite for normal working memory function. By contrast, the marmoset model is sensitive to distractibility commonly observed behaviorally in this species. Surprisingly, this contrasting trend can be swapped by scaling intrafrontal and frontoparietal connections. Finally, the relevance to primate ethology and evolution is discussed. Graphical Abstract HighlightsConsensus mapping allows for directly comparing macaque and marmoset connectomes.Connectomes and spine counts constrain large-scale models of working memory.The marmoset model is susceptible to distraction, but not the macaque.Our results capture real life difference with regard to distraction. 

Abstract The recent publications of the inter-areal connectomes for mouse, marmoset, and macaque cortex have allowed deeper comparisons across rodent vs. primate cortical organization. In general, these show that the mouse has very widespread, “all-to-all” inter-areal connectivity (i.e. a “highly dense” connectome in a graph theoretical framework), while primates have a more modular organization. In this review, we highlight the relevance of these differences to function, including the example of primary visual cortex (V1) which, in the mouse, is interconnected with all other areas, therefore including other primary sensory and frontal areas. We argue that this dense inter-areal connectivity benefits multimodal associations, at the cost of reduced functional segregation. Conversely, primates have expanded cortices with a modular connectivity structure, where V1 is almost exclusively interconnected with other visual cortices, themselves organized in relatively segregated streams, and hierarchically higher cortical areas such as prefrontal cortex provide top–down regulation for specifying precise information for working memory storage and manipulation. Increased complexity in cytoarchitecture, connectivity, dendritic spine density, and receptor expression additionally reveal a sharper hierarchical organization in primate cortex. Together, we argue that these primate specializations permit separable deconstruction and selective reconstruction of representations, which is essential to higher cognition.