How rat brain transform egocentric views into goal-directed navigation behavior?

LaChance, Patrick A., and Jeffrey S. Taube. “A model for transforming egocentric views into goal‐directed behavior.” Hippocampus (2023).

Abstract

Neurons in the rat postrhinal cortex (POR) respond to the egocentric (observer-centered) bearing and distance of the boundaries,

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How spinal circuits implement the locomotor command?

Hsu, LJ., Bertho, M. & Kiehn, O. Deconstructing the modular organization and real-time dynamics of mammalian spinal locomotor networks. Nat Commun 14, 873 (2023). https://doi.org/10.1038/s41467-023-36587-w

Abstract
“Locomotion empowers animals to move. Locomotor-initiating signals from the brain are funneled through …

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How unique and predictable elements of memories are stored and reconstructed by efficiently combining both hippocampal and neocortical systems?

Eleanor Spens, Neil Burgess. A Generative Model of Memory Construction and Consolidation. bioRxiv 2023.01.19.524711; doi: https://doi.org/10.1101/2023.01.19.524711

Abstract
“Human episodic memories are (re)constructed, combining unique features with schema-based predictions, and share neural substrates with imagination. They also show systematic schema-based …

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How the brain maintain and update the uncertainty about one’s location to navigate efficiently?

Yul HR Kang, Daniel M Wolpert, Máté Lengyel. Spatial uncertainty and environmental geometry in navigation. bioRxiv 2023.01.30.526278; doi: https://doi.org/10.1101/2023.01.30.526278

Abstract
Variations in the geometry of the environment, such as the shape and size of an enclosure, have profound

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Whether, and how, replay supports both future planning and preserving memories of the past?

G. Elliott Wimmer, Yunzhe Liu, Daniel C. McNamee, and Raymond J. Dolan. Distinct replay signatures for prospective decision-making and memory preservation. PNAS, 120 (6) e2205211120, 2023. 

Significance
The sequential neural reactivation of prior experience, known as replay, is

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How episodic memories are stored within brains?

Sachin P Vaidya, Raymond A Chitwood, Jeffrey C Magee. The formation of an expanding memory representation in the hippocampus. bioRxiv 2023.02.01.526663; doi: https://doi.org/10.1101/2023.02.01.526663

Abstract
How episodic memories are stored within brains is poorly understood. While certain memory-retaining

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Do artificial intelligence (AI) agents learn to build internal spatial representations (or ‘mental’ maps) of their environment as a natural consequence of learning to navigate?

Erik Wijmans, Manolis Savva, Irfan Essa, Stefan Lee, Ari S. Morcos, Dhruv Batra. Emergence of Maps in the Memories of Blind Navigation Agents. arXiv:2301.13261 [cs.AI], 2023. 

Abstact
“Animal navigation research posits that organisms build and maintain internal spatial representations, …

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How entorhinal grid-like codes and time-locked network dynamics track others navigating through space?

Isabella C. Wagner, Luise P. Graichen, Boryana Todorova, Andre Lüttig, David B. Omer, Matthias Stangl & Claus Lamm. Entorhinal grid-like codes and time-locked network dynamics track others navigating through space. Nat Commun 14, 231 (2023). https://doi.org/10.1038/s41467-023-35819-3

Abstract
Navigating

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How causal inference is performed in attributing retinal motion to self- and object-motion during closed-loop goal-directed navigation?

Jean-Paul Noel, Johannes Bill, Haoran Ding, John Vastola, Gregory C DeAngelis, Dora Angelaki, Jan Drugowitsch. Causal inference during closed-loop navigation: parsing of self- and object-motion. bioRxiv 2023.01.27.525974; doi: https://doi.org/10.1101/2023.01.27.525974

Abstract
A key computation in building adaptive internal models

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How the human brain is tuned to veridical head direction signals?

Benjamin J Griffiths, Thomas Schreiner, Julia Schaefer, Christian Vollmar, Elisabeth Kaufmann, Stefanie Quach, Jan Remi, Soheyl Noachtar, Tobias Staudigl. Electrophysiological signatures of veridical head direction in humans. bioRxiv 2023.01.26.525724; doi: https://doi.org/10.1101/2023.01.26.525724

Abstract
“Information about heading direction is critical for …

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How navigation and memory processes interact in humans?

Thomas Schreiner, Benjamin J. Griffiths, Merve Kutlu, Christian Vollmar, Elisabeth Kaufmann, Stefanie Quach, Jan Remi, Soheyl Noachtar, Tobias Staudigl. Memory reactivation of real-world spatial orientation revealed by human electrophysiology. bioRxiv 2023.01.27.525854; doi: https://doi.org/10.1101/2023.01.27.525854

Abstract
Spatial navigation and memory

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What are the brain mechanisms underlying spatial navigation in birds?

Agarwal A, Sarel A, Derdikman D, Ulanovsky N, Gutfreund Y. Spatial coding in the hippocampus and hyperpallium of flying owls. Proceedings of the National Academy of Sciences. 2023 Jan 31;120(5):e2212418120.

Significance
Birds travel long distances and navigate in

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How retrosplenial cortex computes heading direction from landmark information?

Eleonora Lomi, Kate Jeffery, Anna Mitchell. Convergence of direction, location and theta in the rat anteroventral thalamic nucleus. bioRxiv 2023.01.11.523585; doi: https://doi.org/10.1101/2023.01.11.523585

Abstract
Retrosplenial cortex (RSC) is a cortical region that computes heading direction from landmark information, but

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How the hippocampus incorporates new contextual information into a previously formed and stabilized spatial representation?

Jake Ormond, Simon A. Serka, Joshua P. Johansen. Enhanced reactivation of remapping place cells during aversive learning. Journal of Neuroscience 3 January 2023, JN-RM-1450-22; DOI: 10.1523/JNEUROSCI.1450-22.2022

Abstract
Study of the hippocampal place cell system has greatly enhanced our

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Whether hippocampal time cells represent context-dependent experience or time per se?

David B. Omer, Liora Las & Nachum Ulanovsky. Contextual and pure time coding for self and other in the hippocampus. Nat Neurosci (2022). https://doi.org/10.1038/s41593-022-01226-y

Abstract
“Navigation and episodic memory depend critically on representing temporal sequences. Hippocampal ‘time cells’ form

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