Visual mental imagery (VMI) decoding uses brain activity to reconstruct internally generated visual scenes, providing a potential pathway for externalizing internal experiences and developing neuroprosthetic communication interfaces. However, progress is limited by the lack of dedicated, training-scale VMI datasets. Current VMI paradigms often rely on visual prompts or short-term memory images, introducing visual and mnemonic confounds that make it difficult to disentangle neural activity associated with endogenous image construction from signals driven by prior or concurrent visual input. Furthermore, existing VMI datasets offer limited descriptive control over individual visual attributes, making it difficult to systematically assess fine grained visual details. To address these gaps, we introduce AVID, the first dedicated training-scale 5.0 Tesla functional magnetic resonance imaging (fMRI) resource for auditory-induced VMI decoding. AVID comprises approximately 67 hours of dense recordings from nine participants. The dataset is structured into two complementary splits: a scene-level complex split using naturalistic Mandarin descriptions and a controlled simple split with explicitly specified visual attributes. We further formalize a standardized evaluation protocol that decouples source-image consistency from semantic alignment, allowing for a more nuanced assessment of imagery reconstruction. Baseline qualitative and quantitative results show that current reconstruction pipelines remain limited on AVID, although the most successful reconstructions preserve recognizable scene level semantics from spoken descriptions. By combining dedicated training-scale neural recordings and standardized evaluation resources, AVID provides both a data foundation for imagery-specific model development and a benchmark for evaluating VMI decoding with substantially reduced sensory contamination.
Figures & tables
Figure 1: Overview of our benchmark. (A) Source images are converted into spoken Mandarin descriptions, which participants hear during eyes-closed imagery in the 5T scanner. The fMRI data are preprocessed to estimate trial-wise responses and define ROI-based neural inputs for decoding. (B) AVID includes approximately 67 hours of recordings from 9 participants across complex scene-level and controlled attribute splits, using a trial structure with an auditory cue, imagery period, vividness rating, and reset interval. (C) Decoders are evaluated on fixed AVID splits, with reconstructions scored by source-image consistency and spoken-description alignment.
Split
Participants
Stimuli
Total trials
Task time (h)
Repetitions
Complex
9
800
14,400
48.0
2
Simple
7
400
5,600
18.7
2
Total
9
1,200
20,000
66.7
2
Table 1: Summary of AVID dataset statistics.
Figure 2: Qualitative comparison of mental imagery generation results. (A) Examples from the complex stimuli split. (B) Examples from the simple stimuli split. For each stimulus, we compare the source image with reconstructions generated by LDM, MindEye1, MindEye2, and MindBridge. The results illustrate how different methods recover semantic content and visual structure across natural images and simple shape stimuli.
Image-image
Image-text
Method
PixCorr
SSIM
Inception
CLIP-I
CLIP-T
SigLIP
AltCLIP
TIFA
LDM
0.038
0.185
59.09%
59.61%
66.81%
68.54%
67.34%
32.56%
MindEye1
0.056
0.291
65.14%
65.94%
67.83%
70.63%
69.83%
30.27%
MindEye2
0.034
0.262
55.75%
57.81%
57.95%
59.08%
58.82%
24.34%
MindBridge
0.040
0.170
65.22%
65.80%
67.66%
69.20%
69.61%
32.25%
Table 2: Complex split baseline results. Metrics are grouped by source image consistency and spoken description alignment.
Image-image
Image-text
Method
PixCorr
SSIM
Inception
CLIP-I
CLIP-T
SigLIP
AltCLIP
TIFA
LDM
-0.001
0.636
54.07%
51.75%
55.59%
57.16%
57.25%
48.92%
MindEye1
-0.028
0.962
53.19%
52.75%
53.19%
54.33%
52.83%
44.34%
MindEye2
0.004
0.684
53.54%
51.41%
52.09%
52.81%
51.53%
39.34%
MindBridge
-0.006
0.906
57.49%
55.69%
55.69%
57.13%
56.69%
40.32%
Table 3: Simple split baseline results. Metrics are grouped by source image consistency and spoken description alignment.
Method
Color
Position
Visual identity
LDM
30.13±5.58%
24.07±5.46%
2.36±1.79%
MindEye1
31.65±7.83%
35.34±8.56%
3.38±1.96%
MindEye2
32.59±10.47%
29.39±4.73%
2.07±1.25%
MindBridge
35.55±4.04%
26.99±6.81%
2.70±1.30%
Chance
25.76%
20.00%
1.05%
Table 4: Attribute-level evaluation on the simple split. Reconstruction scores are class-balanced accuracies, reported as mean ± sample standard deviation across seven participants. The chance row gives the analytical expected score under uniform selection from the corresponding answer options. Differences between model configurations are descriptive.
Appendix figures & tables19 assets
Supplementary material from the paper’s appendix.
Appendix
Figure 3: Countdown screenshot.
Table 5: Example complex stimuli.
Table 6: Example simple stimuli.
Figure 4: Temporal signal-to-noise ratio (tSNR) across subjects and runs in AVID. (A) Distribution of run-wise median tSNR values for each subject, where tSNR was computed voxel-wise after quadratic detrending and summarized within the top 10% highest-tSNR voxels in each run. (B) Run-by-run median tSNR trajectories for all subjects, with colored lines indicating individual subjects and the black line indicating the across-subject median. The dashed vertical line separates complex runs from simple runs.
Figure 5: Cortical distribution of noise ceilings, shown in left lateral, ventral, and right lateral views. Colors indicate the estimated percentage of explainable variance in the mean response across two stimulus repetitions. Gray shading depicts cortical anatomy.
Split
Cortical region
Low-vividness NC
High-vividness NC
p
Complex
Postcentral gyrus
8.21±2.46 %
11.55±2.64 %
0.0039
Superior temporal gyrus
12.38±1.20 %
13.89±2.16 %
0.0273
Fusiform gyrus
10.57±3.43 %
10.42±2.84 %
0.8203
Pars orbitalis
8.75±1.68 %
9.22±1.88 %
0.3594
Simple
Postcentral gyrus
8.94±2.40 %
9.69±2.00 %
0.0781
Superior temporal gyrus
12.08±1.42 %
12.06±2.42 %
1.0000
Appendix
Table 7: Neural response reliability for the 100 lowest- and 100 highest-vividness stimuli selected separately within each participant and split. Values are across-participant mean ± sample standard deviation of noise-ceiling estimates. The complex and simple splits included nine and seven participants, respectively. p values were obtained using two-sided paired Wilcoxon signed-rank tests.
Attribute
fMRI accuracy
Chance
Gaussian control
t -test p
Wilcoxon p
Color
0.395±0.021
0.333
0.332±0.031
0.00012
0.0078
Position
0.440±0.144
0.200
0.200±0.031
0.0022
0.0078
Appendix
Table 8: Direct attribute decoding from simple-split fMRI responses and Gaussian-feature controls. fMRI accuracies are means ± sample SD across seven participants; Gaussian values summarize the random-feature control. The p values compare participant-level fMRI accuracies with nominal chance and are uncorrected.
Input
BLEU-1
BLEU-4
ROUGE-L F1
Token-F1
Real fMRI
0.2236±0.0199
0.0759±0.0079
0.2522±0.0137
0.2961±0.0193
Gaussian fMRI
0.2049±0.0075
0.0609±0.0025
0.2298±0.0050
0.2756±0.0033
Shuffled fMRI
0.1924±0.0031
0.0608±0.0014
0.2266±0.0038
0.2645±0.0032
Appendix
Table 9: fMRI-to-text decoding with neural-input controls. Values are means ± sample SD across nine participants. Bold indicates significantly higher performance than both controls after Holm correction.
Metric
Real fMRI
Shuffled-fMRI chance
PixCorr
0.0562±0.0245
0.0272±0.0072
SSIM
0.2910±0.0074
0.2828±0.0013
CLIP-I 2WC
65.94±8.20%
50.02±0.91%
Inception 2WC
65.14±8.86%
49.82±1.03%
CLIP-T 2WC
67.83±8.81%
49.90±0.96%
SigLIP 2WC
70.63±10.59%
49.99±0.22%
Appendix
Table 10: MindEye1 reconstruction with real and shuffled fMRI on the complex split. Real-fMRI values are means ± sample SD across nine participants; shuffled-fMRI values are means ± SD across 50 group-level shuffle repetitions. Two-way identification accuracies are reported as percentages. Bold indicates significant real-fMRI performance under a one-sided empirical permutation test.
Table 11: Representative evaluator errors on original reference images. The evaluator correctly identifies color and spatial position but misclassifies semicircle orientation. Identity answers are abbreviated to the straight-edge direction; the full answer format is “semicircle (straight edge at [direction])”. Reference descriptions are shown for illustration and are not provided to the evaluator.
Split
Speech ROI
Language ROI
Remaining ROI
Complex
1,426±933
2,191±2,153
38,538±5,900
Simple
1,561±1,024
2,348±2,460
37,537±6,344
Appendix
Table 12: ROI sizes after NC-based vertex selection. Values are the mean ± sample standard deviation of vertex counts across participants (complex: n=9 ; simple: n=7 ). The top 15% were selected separately within each candidate region.
Metric
Speech ROI
Language ROI
Remaining ROI
vs. Speech
vs. Language
PixCorr
0.046±0.019
0.049±0.026
0.061±0.024
0.0747
0.0915
SSIM
0.327±0.028
0.296±0.011
0.291±0.011
0.9976
0.8892
CLIP-I 2WC
0.538±0.064
0.613±0.069
0.657±0.083
0.0011
0.0136
Inception 2WC
0.537±0.062
0.602±0.081
0.648±0.092
0.0030
0.0257
CLIP-T R@1
0.013±0.013
0.026±0.032
0.035±0.039
0.0488
0.1294
CLIP-T R@5
0.057±0.055
0.092±0.083
0.147±0.105
0.0056
0.0070
Appendix
Table 13: ROI-restricted MindEye1 reconstruction performance on the complex split ( n=9 ). Values are the mean ± sample standard deviation across participants. The final two columns report Benjamini–Hochberg-adjusted p -values from one-sided paired t -tests assessing whether the remaining ROI outperformed the respective comparison ROI. Correction was applied jointly across all 20 comparisons; adjusted p<0.05 indicates significant superiority.
Figure 6: Qualitative comparison of mental imagery generation results for ROI sensitivity analysis. (A) Examples from the complex stimuli split. (B) Examples from the simple stimuli split. For each stimulus, we compare the source image with reconstructions generated by LDM, MindEye1, MindEye2, and MindBridge. The results illustrate how different methods recover semantic content and visual structure across natural images and simple shape stimuli.
Image-image
Image-text
Method
PixCorr
SSIM
Inception
CLIP-I
CLIP-T
SigLIP
AltCLIP
TIFA
LDM
0.040
0.187
58.30%
59.36%
67.42%
68.30%
68.09%
31.99%
MindEye1
0.061
0.291
64.85%
65.71%
68.06%
70.04%
70.33%
30.91%
MindEye2
0.031
0.265
55.06%
56.75%
55.77%
57.85%
57.06%
24.62%
MindBridge
0.040
0.170
63.69%
64.78%
66.70%
67.82%
68.50%
32.06%
Appendix
Table 14: Complex split baseline results under NSL. Metrics are grouped by source image consistency and spoken description alignment.
Image-image
Image-text
Method
PixCorr
SSIM
Inception
CLIP-I
CLIP-T
SigLIP
AltCLIP
TIFA
LDM
-0.006
0.636
51.90%
52.31%
55.69%
57.12%
56.87%
48.42%
MindEye1
-0.031
0.963
52.35%
51.10%
51.45%
51.15%
51.84%
44.82%
MindEye2
0.003
0.679
54.39%
53.93%
52.04%
53.07%
52.85%
41.15%
MindBridge
-0.008
0.916
56.84%
55.53%
54.72%
57.58%
54.59%
40.61%
Appendix
Table 15: Simple split baseline results under NSL. Metrics are grouped by source image consistency and spoken description alignment.
Method
PixCorr
SSIM
Inception
CLIP-I
Complex split: NS input
LDM
0.038±0.014
0.185±0.005
59.10±5.00%
59.60±4.90%
MindEye1
0.056±0.025
0.291±0.007
65.10±8.90%
65.90±8.20%
MindEye2
0.034±0.017
0.262±0.018
55.70±4.70%
57.80±4.30%
MindBridge
0.040±0.006
0.170±0.006
65.20±6.50%
65.80±7.00%
Simple split: NS input
Appendix
Table 16: Participant-level variability in source-image consistency metrics. Values are mean ± sample SD across nine participants for the complex split and seven for the simple split. Inception and CLIP-I scores are reported as percentages. Bold marks the highest mean within each split and input setting. NS denotes ROIm∖ROIs , and NSL denotes ROIm∖(ROIs∪ROIl) .
Method
CLIP-T
SigLIP
AltCLIP
TIFA
Complex split: NS input
LDM
66.80±8.30%
68.50±7.60%
67.30±8.40%
32.60±4.40%
MindEye1
67.80±8.80%
70.63±10.59%
69.80±9.60%
30.30±4.90%
MindEye2
57.90±5.30%
59.10±5.90%
58.80±6.50%
24.30±1.90%
MindBridge
67.70±7.00%
69.20±7.20%
69.60±7.50%
32.30±3.30%
Simple split: NS input
Appendix
Table 17: Participant-level variability in spoken-description alignment metrics. All metrics are reported as percentages, with values given as mean ± sample SD across nine participants for the complex split and seven for the simple split. Bold marks the highest mean within each split and input setting. NS and NSL follow Table 16 .
Baseline
Training setting
Primary input ROI
Model fitting and reconstruction
LDM
Single-subject
ROIm∖ROIs
Ridge regression with 5-fold cross-validation over the regularization grid; Stable Diffusion reconstruction with 50 denoising steps, guidance scale 7.5, and img2img strength 0.8.
MindEye1
Single-subject
ROIm∖ROIs
Subject-specific training for 240 epochs with CLIP ViT-L/14 targets; MindEye1 reconstruction and candidate-selection pipeline.
MindEye2
Leave-one-participant-out transfer
ROIm∖ROIs
Joint training on non-target participants for 150 epochs, followed by 15 epochs of target-participant fine-tuning; diffusion-prior and blurry reconstruction branches.
MindBridge
Multi-participant joint training
ROIm∖ROIs
Joint training for 600 epochs with reconstruction and cycle-consistency objectives.
Appendix
Table 18: Summary of baseline configurations. The primary input ROI is ROIm∖ROIs for all four methods. Detailed hyperparameters are provided in the model-specific descriptions above; the additional speech/language-excluded input is evaluated in the ROI sensitivity analysis.
Family
Training identities
Validation identities
Letter
F, G, H, J, K, Q, W, X, Y (9)
C, S (2)
Single digit
0, 1, 2, 3, 4, 6, 7, 9 (8)
5, 8 (2)
Digits
103, 194, 372, 431, 566, 653, 740, 918 (8)
286, 829 (2)
Shape
Circle; cross; diamond; five-pointed star; ring; square; three-by-three dot array; triangle; vertical rectangle; semicircles with the straight edge at the bottom, left, or right (12)
Heart; horizontal rectangle; semicircle with the straight edge at the top (3)
Table 19: Identity membership of the additional visual-identity-disjoint split. Counts in parentheses indicate the number of identities. Semicircles are described by the location of their straight edge.
Recent progress in visual brain decoding from fMRI has been enabled by large-scale datasets such as the Natural Scenes Dataset (NSD) and powerful diffusion-based generative models. While current pipelines are primarily optimized for perception, their performance under mental-imagery remains less well understood. In this work, we study how a state-of-the-art (SOTA) perception decoder (DynaDiff) can be adapted to reconstruct imagined content from the NSD-Imagery benchmark. We propose a latent functional alignment (LFA) approach that maps imagery-evoked activity to the pretrained model's semantic content-enriched conditioning space, by adding a simple alignment module, while keeping the original remaining components frozen. To mitigate the limited amount of matched imagery-perception supervision, we further introduce a neural retrieval-based augmentation strategy that selects semantically related NSD perception trials from the same participants. Across four subjects, LFA consistently improves high-level semantic reconstruction metrics relative to the frozen pretrained baseline and a voxel-space ridge alignment baseline, and enables above-chance decoding from multiple cortical regions. These results suggest that semantic structure learned from perception can be leveraged to stabilize and improve visual imagery decoding under out-of-distribution conditions.
Fabrizio Spera, Tommaso Boccato, Michal Olak +2
Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy · Tether Evo · A.A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, USA
To be useful for downstream applications, vision decoding models that are trained to reconstruct seen images from human brain activity must be able to generalize to internally generated visual representations, i.e., mental images. In an analysis of the recently released NSD-Imagery dataset, we demonstrated that while some modern vision decoders can perform quite well on mental image reconstruction, some fail, and that state-of-the-art (SOTA) performance on seen image reconstruction is no guarantee of SOTA performance on mental image reconstruction. Motivated by these findings, we developed MIRAGE, a method explicitly designed to train on vision datasets and cross-decode mental images from brain activity. MIRAGE employs a linear backbone and multi-modal text and image features as input to a diffusion model. Feature metrics and human raters establish MIRAGE as SOTA for mental image reconstruction on the NSD-Imagery benchmark. With ablation analysis we show that mental image reconstruction works best when decoders use image features with relatively few dimensions and include guidance from text-based and both high- and low-level image-based features. Our work indicates that--given the right architecture--existing large-scale datasets using external stimuli are viable training data for decoding mental images, and warrant optimism about the future success and utility of mental image reconstruction.
Reese Kneeland, Cesar Kadir Torrico Villanueva, Jordyn Ojeda +4
University of Minnesota, Minneapolis, Minnesota, United States of America · Medical AI Research Center (MedARC) · Stanford University, Palo Alto, California, United States of America +2
Decoding visual content from fMRI signals recorded while a person views images, and specifically answering questions about the seen images, is a long-standing challenge. While significant progress has been made in recent years in visual question answering (VQA) from fMRI, performance remains limited. Moreover, although recent models can make increasingly accurate predictions, they have rarely been used as tools for understanding the structure of visual representations in the brain. We present Brain-IT-VQA, a framework for visual question answering from fMRI. Building on the Brain Interaction Transformer (Brain-IT), our method decodes language tokens from brain activity and integrates them with a language model to answer visual questions. Our model substantially outperforms previous fMRI-based captioning and VQA approaches. We further introduce NSD-VQA, a new dataset and benchmark for visual question answering from fMRI. Unlike existing image-fMRI VQA datasets, which typically provide only a few broad and weakly controlled questions per image, NSD-VQA provides on average 20 question-answer pairs per image across 20 controlled question categories that disentangle multiple levels of visual understanding. This enables more reliable and interpretable evaluation despite limited fMRI test data. Together, Brain-IT-VQA and NSD-VQA provide both a strong predictive framework and a tool for studying brain representations. Using this benchmark, we quantify which forms of visual and semantic information can be reliably decoded from fMRI responses to natural images. We further analyze the contributions of different brain regions across question types.
Roman Beliy, Matias Cosarinsky, Oliver Heinimann +2