Journal Article10.1038/s41467-024-49823-8
Hippocampal connectivity patterns echo macroscale cortical evolution in the primate brain
Nicole Eichert,Jordan DeKraker,Amy FD Howard,I Huszár,Silei Zhu,Jérôme Sallet,Karla L. Miller,Rogier B. Mars,Saâd Jbabdi,Boris C. Bernhardt +9 more
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TL;DR: This study examines the evolution of the hippocampus in primates, revealing a balance between structural preservation and functional reconfiguration, with anterior-posterior organisation conserved across species, but functional integration varying between humans and macaques.
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Abstract: While the hippocampus is key for human cognitive abilities, it is also a phylogenetically old cortex and paradoxically considered evolutionarily preserved. Here, we introduce a comparative framework to quantify preservation and reconfiguration of hippocampal organisation in primate evolution, by analysing the hippocampus as an unfolded cortical surface that is geometrically matched across species. Our findings revealed an overall conservation of hippocampal macro- and micro-structure, which shows anterior-posterior and, perpendicularly, subfield-related organisational axes in both humans and macaques. However, while functional organisation in both species followed an anterior-posterior axis, we observed a marked reconfiguration in the latter across species, which mirrors a rudimentary integration of the default-mode-network in non-human primates. Here we show that microstructurally preserved regions like the hippocampus may still undergo functional reconfiguration in primate evolution, due to their embedding within heteromodal association networks.
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Hippocampal connectivity patterns echo macroscale cortical evolution in the primate brain
Nicole Eichert,Jordan DeKraker,Amy FD Howard,I Huszár,Silei Zhu,Jérôme Sallet,Karla L. Miller,Rogier B. Mars,Saâd Jbabdi,Boris C. Bernhardt +9 more
TL;DR: This study examines the evolution of the hippocampus in primates, revealing a balance between structural preservation and functional reconfiguration, with anterior-posterior organisation conserved across species, but functional integration varying between humans and macaques.
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HippoMaps: multiscale cartography of human hippocampal organization
Jordan DeKraker,Donna Gift Cabalo,Jessica Royer,Alexander Ngo,Ali R. Khan,Bradley G Karat,Oualid Benkarim,Raúl Rodríguez-Cruces,Birgit Frauscher,Raluca Pana,Justine Y. Hansen,Bratislav Misic,Sofie L. Valk,Jonathan C. Lau,Matthias Kirschner,Andrea Bernasconi,Neda Bernasconi,Sascha E.A. Muenzing,Markus Axer,Katrin Amunts,Alan C. Evans,Boris C. Bernhardt,Jordan DeKraker,Donna Gift Cabalo,Jessica Royer,Alexander Ngo,Ali R. Khan,Bradley G Karat,Oualid Benkarim,Raúl Rodríguez-Cruces,Birgit Frauscher,Raluca Pana,Justine Y. Hansen,Bratislav Misic,Sofie L. Valk,Jonathan C. Lau,Matthias Kirschner,Andrea Bernasconi,Neda Bernasconi,Sascha E.A. Muenzing,Markus Axer,Katrin Amunts,Alan C. Evans,Boris C. Bernhardt +43 more
TL;DR: HippoMaps is an open-access toolbox and data warehouse for mapping and contextualizing subregional hippocampal data, integrating 3D histology, MRI, and iEEG recordings, with tools for spatial map analysis and autocorrelation correction.
Spatial and semantic memory reorganize a hippocampal long-axis gradient
Joel L. Voss,James E Kragel,Joel L. Voss,James E Kragel +3 more
- 15 Oct 2025
Abstract: Abstract The hippocampus supports episodic memory by binding spatial and semantic information, yet how this information is simultaneously organized along its long axis remains debated. Gradient accounts propose a continuous shift in representational scale, from coarse coding in anterior to fine coding in posterior regions, whereas modular accounts posit discrete subregions specialized for distinct functions. Using high-resolution fMRI together with eye tracking as a readout of spatial and semantic memory during sequence learning, we directly tested these competing models. During predictable sequences, hippocampal activity continuously varied along the long axis. In contrast, modular organization emerged when sequences mismatched memory. Subregions in the anterior and posterior hippocampus were sensitive to semantic and spatial mismatches, respectively. Notably, the intermediate hippocampus was specifically sensitive to concurrent mismatches in both dimensions, but not to mismatches in either dimension alone. These content-sensitive subregions were embedded within distinct cortical networks that reorganized according to memory demands. Together, our findings show the hippocampus flexibly combines gradient and modular dynamics to simultaneously represent the spatial and semantic content that defines episodic memory.
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