A prevalent model is that sharp-wave ripples (SWR) arise ‘spontaneously’ in CA3 and propagate recent memory traces outward to the neocortex to facilitate memory consolidation there. Using voltage and extracellular glutamate transient recording over widespread regions of mice dorsal neocortex in relation to CA1 multiunit activity (MUA) and SWR, we find that the largest SWR-related modulation occurs in retrosplenial cortex; however, contrary to the unidirectional hypothesis, neocortical activation exhibited a continuum of activation timings relative to SWRs, varying from leading to lagging. Thus, contrary to the model in which SWRs arise ‘spontaneously’ in the hippocampus, neocortical activation often precedes SWRs and may thus constitute a trigger event in which neocortical information seeds associative reactivation of hippocampal ‘indices’. This timing continuum is consistent with a dynamics in which older, more consolidated memories may in fact initiate the hippocampal-neocortical dialog, whereas reactivation of newer memories may be initiated predominantly in the hippocampus.

Brain areas within the lateral parietal cortex (LPC) and ventral temporal cortex (VTC) have been shown to code for abstract quantity representations and for symbolic numerical representations, respectively. To explore the fast dynamics of activity within each region and the interaction between them, we used electrocorticography recordings from 16 neurosurgical subjects implanted with grids of electrodes over these two regions and tracked the activity within and between the regions as subjects performed three different numerical tasks. Although our results reconfirm the presence of math-selective hubs within the VTC and LPC, we report here a remarkable heterogeneity of neural responses within each region at both millimeter and millisecond scales. Moreover, we show that the heterogeneity of response profiles within each hub mirrors the distinct patterns of functional coupling between them. Our results support the existence of multiple bidirectional functional loops operating between discrete populations of neurons within the VTC and LPC during the visual processing of numerals and the performance of arithmetic functions. These findings reveal information about the dynamics of numerical processing in the brain and also provide insight into the fine-grained functional architecture and connectivity within the human brain.A lthough the ability to approximate or compare rough quantities is present even in human infants (1) and in other species such as nonhuman primates (2-4) and birds (5), the association of exact quantities with symbols (e.g., the numeral "10") or verbal representations (e.g., the word "ten") is unique to humans exposed to such culturally learned entities (6-8). Moreover, dissociable number-and quantity-related behavioral deficits (i.e., deficits relating to symbolic or verbal numerical representations versus abstract quantity representations) are associated with different lesion locations within the brain (9-14). These observations in part motivated the Triple Code model positing that the human brain contains three different numerical representations: symbolic, verbal, and abstract quantity, each coded in a different brain region (15,16). The model also predicts that, depending on task demands (e.g., simple visual recognition of a numeral versus determining the larger of two numerals versus verbal naming of a numeral), all or a subset of these brain regions interact with each other (15, 16).Neuroimaging, electrophysiology, and lesion studies in both humans and nonhuman primates have long implicated the parietal lobe, particularly the anterior segment of the intraparietal sulcus (aIPS), in abstract quantity representations irrespective of the modality of presentation (e.g., "4" vs. "four" vs. "::"), with specific neurons or neuronal populations exhibiting tuning around a preferred numerosity (4, 17-25). Moreover, brain activity within this region and its functional and anatomical connectivity with other brain regions are correlated with mathematical performance in individual subjects (26)(27)(28)(29),...

Keywords 19Hippocampus, neocortex, hippocampal-cortical interaction, memory consolidation, sharp-wave 20 ripple, multi-unit activity, wide-field mesoscale optical imaging, local field potential, head-21 restrained sleep 22 23 24 25Abstract 26A prevalent model is that sharp-wave ripples (SWR) arise 'spontaneously' in CA3 and 27 propagate recent memory traces outward to the neocortex to facilitate memory consolidation 28 there. Using voltage and extracellular glutamate transient recording over widespread regions of 29 mice dorsal neocortex in relation to CA1 multiunit activity (MUA) and SWR, we find that the 30 largest SWR-related modulation occurs in retrosplenial cortex; however, contrary to the 31 unidirectional hypothesis, neocortical activation exhibited a continuum of activation timings 32 relative to SWRs, varying from leading to lagging. Thus, contrary to the model in which SWRs 33 arise 'spontaneously' in the hippocampus, neocortical activation often precedes SWRs and may 34 thus constitute a trigger event in which neocortical information seeds associative reactivation of 35

The insulo-opercular network functions critically not only in encoding taste, but also in guiding behavior based on anticipated food availability. However, there remains no direct measurement of insulo-opercular activity when humans anticipate taste. Here, we collect direct, intracranial recordings during a food task that elicits anticipatory and consummatory taste responses, and during ad libitum consumption of meals. While cue-specific high-frequency broadband (70–170 Hz) activity predominant in the left posterior insula is selective for taste-neutral cues, sparse cue-specific regions in the anterior insula are selective for palatable cues. Latency analysis reveals this insular activity is preceded by non-discriminatory activity in the frontal operculum. During ad libitum meal consumption, time-locked high-frequency broadband activity at the time of food intake discriminates food types and is associated with cue-specific activity during the task. These findings reveal spatiotemporally-specific activity in the human insulo-opercular cortex that underlies anticipatory evaluation of food across both controlled and naturalistic settings.