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. 2024 Jan 18;27(3):547–560. doi: 10.1038/s41593-023-01554-7

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — a, For each cortical area in each monkey and each study, across-probes mean relative power map (left) and mean relative power in the alpha-beta (blue) and gamma (red) bands as a function of laminar depth with respect to the alpha-beta/gamma crossover channel (right). b, The percentage of probes with an identifiable alpha-beta/gamma crossover using different identification methods: manual, FLIP and vFLIP. Light gray bars, percentage of identifiable probes after shuffling channel positions. c, Mean IS across all comparisons within area (n = 14), between areas (n = 18), within monkey (n = 32), between monkeys (n = 25), within study (n = 18) and between studies (n = 12). Data points for all comparisons are shown. Error bars, mean ± s.e.m. across all (independent) comparisons. Two-tailed unpaired t-tests were used to compare within versus between areas (P = 0.0029), within versus between monkeys (P = 0.15) and within versus between studies (P = 0.019). *, significant difference; NS, not significant.