Presented During:
Thursday, June 26, 2025: 11:30 AM - 12:45 PM
Brisbane Convention & Exhibition Centre
Room:
M4 (Mezzanine Level)
Poster No:
828
Submission Type:
Abstract Submission
Authors:
KAIXIANG ZHUANG1, Xinyu Liang1, Yun Wang1, Joern Alexander Quent1, Deniz Vatansever1
Institutions:
1Fudan University, Shanghai, Shanghai
First Author:
Co-Author(s):
Yun Wang
Fudan University
Shanghai, Shanghai
Introduction:
Humans excel at organizing high-dimensional conceptual information into low-dimensional semantic spaces [1], facilitating complex mental operations such as analogical reasoning, inferences and generalization [2]. Despite extensive behavioral evidence for this compression process, its neural basis and cortical topography remain largely unexplored. Using ultra-high resolution 7T fMRI and a comprehensive set of 1,854 object concepts, here we investigated how cortical responses represent and compress semantic information into low-dimensional manifolds. Our results highlight the default mode network (DMN) as a critical hub for semantic compression, providing novel insights into how humans efficiently organize and utilize conceptual knowledge [3].
Methods:
We presented 22,256 high-quality object-centric images, representing 1,854 concepts from the THINGS database [4], to 20 participants (24.56 ± 2.42 years, 14F/6M) during 7T fMRI across five consecutive sessions (60 runs in total) (Fig. 1a). A vertex-by-concept embedding matrix was constructed by averaging GLMsingle-derived single-trial beta maps across images and participants (Fig. 1b). Dimensionality reduction using Principal Component Analysis (PCA) uncovered cortical manifolds of conceptual information, which we interpreted via 66 behaviorally-driven semantic dimensions [5] and 53 semantic categories [6]. Cortical semantic compressibility was assessed by mapping vertex-wise reconstruction errors, with lower errors indicating greater alignment to low-dimensional representations (Fig. 1c-d).
Results:
The posterior DMN, including the PCC, TPJ, and IPL, demonstrated maximal semantic compressibility, reflecting stronger alignment with low-dimensional cortical semantic manifolds (Fig. 1e). In contrast, regions such as the OFC, temporal area TF, and primary visual cortex showed minimal compressibility, indicating more specialized representations. At the macro-scale, transmodal networks associated with higher-order cognition (e.g., DMN, frontoparietal networks) exhibited greater compressibility than unimodal sensorimotor networks (e.g., auditory and language networks) (Fig. 1f). Compressed cortical semantic manifolds aligned closely with behaviorally-driven dimensions (Fig. 2a), enabling flexible delineation of semantic categories (Fig. 2b) and encoding multiple pathways of conceptual access in the posterior DMN (Fig. 2c).
Conclusions:
Our findings elucidate the neural mechanisms of semantic compression, identifying the posterior DMN as a central hub for transforming high-dimensional conceptual information into low-dimensional semantic manifolds. These manifolds not only align with human-interpretable dimensions but also enable flexible categorical access via diverse representational pathways, advancing our understanding of the cortical organization of conceptual knowledge for healthy and adaptive cognition.
Higher Cognitive Functions:
Higher Cognitive Functions Other 2
Language:
Language Comprehension and Semantics
Learning and Memory:
Long-Term Memory (Episodic and Semantic)
Learning and Memory Other 1
Modeling and Analysis Methods:
Multivariate Approaches
Keywords:
Cognition
Cortex
Data analysis
Design and Analysis
Experimental Design
FUNCTIONAL MRI
Memory
Multivariate
1|2Indicates the priority used for review
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Please indicate below if your study was a "resting state" or "task-activation” study.
Task-activation
Healthy subjects only or patients (note that patient studies may also involve healthy subjects):
Healthy subjects
Was this research conducted in the United States?
No
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
NOTE: Any human subjects studies without IRB approval will be automatically rejected.
Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
NOTE: Any animal studies without IACUC approval will be automatically rejected.
Not applicable
Please indicate which methods were used in your research:
Functional MRI
Behavior
For human MRI, what field strength scanner do you use?
7T
Provide references using APA citation style.
[1] Huth, A. G., De Heer, W. A., Griffiths, T. L., Theunissen, F. E., & Gallant, J. L. (2016). Natural speech reveals the semantic maps that tile human cerebral cortex. Nature, 532(7600), 453-458.
[2] Hebart, M. N., Zheng, C. Y., Pereira, F., & Baker, C. I. (2020). Revealing the multidimensional mental representations of natural objects underlying human similarity judgements. Nature human behaviour, 4(11), 1173-1185.
[3] Bottini, R., & Doeller, C. F. (2020). Knowledge across reference frames: Cognitive maps and image spaces. Trends in Cognitive Sciences, 24(8), 606-619.
[4] Hebart, M. N., Dickter, A. H., Kidder, A., Kwok, W. Y., Corriveau, A., Van Wicklin, C., & Baker, C. I. (2019). THINGS: A database of 1,854 object concepts and more than 26,000 naturalistic object images. PloS one, 14(10), e0223792.
[5] Contier, O., Baker, C. I., & Hebart, M. N. (2024). Distributed representations of behaviour-derived object dimensions in the human visual system. Nature Human Behaviour, 8(11), 2179-2193.
[6] Stoinski, L. M., Perkuhn, J., & Hebart, M. N. (2024). THINGSplus: New norms and metadata for the THINGS database of 1854 object concepts and 26,107 natural object images. Behavior Research Methods, 56(3), 1583-1603.
No