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Resolving human object recognition in space and time


A comprehensive picture of object processing in the human brain requires combining both spatial and temporal information about brain activity. Here we acquired human magnetoencephalography (MEG) and functional magnetic resonance imaging (fMRI) responses to 92 object images. Multivariate pattern classification applied to MEG revealed the time course of object processing: whereas individual images were discriminated by visual representations early, ordinate and superordinate category levels emerged relatively late. Using representational similarity analysis, we combined human fMRI and MEG to show content-specific correspondence between early MEG responses and primary visual cortex (V1), and later MEG responses and inferior temporal (IT) cortex. We identified transient and persistent neural activities during object processing with sources in V1 and IT. Finally, we correlated human MEG signals to single-unit responses in monkey IT. Together, our findings provide an integrated space- and time-resolved view of human object categorization during the first few hundred milliseconds of vision.

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Figure 1: Decoding of images from MEG signals.
Figure 2: Time course of decoding category membership of individual objects.
Figure 3: Dynamics of visual representations across time.
Figure 4: Relating MEG and fMRI signals in V1 and IT.
Figure 5: Relating MEG and fMRI signals across time.
Figure 6: Relating human MEG to electrophysiological signals in monkey IT.

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This work was funded by US National Eye Institute grant EY020484 (to A.O.), US National Science Foundation grant BCS-1134780 (to D.P.) and a Humboldt Scholarship (to R.M.C.), and was conducted at the Athinoula A. Martinos Imaging Center at the McGovern Institute for Brain Research, Massachusetts Institute of Technology.

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Authors and Affiliations



R.M.C., D.P. and A.O. designed the research. R.M.C. and D.P. performed experiments and analyzed the data. R.M.C., D.P. and A.O. wrote the manuscript.

Corresponding author

Correspondence to Radoslaw Martin Cichy.

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The authors declare no competing financial interests.

Integrated supplementary information

Supplementary Figure 1 Experimental design in MEG, fMRI and behavioral experiments.

Participants (n = 16) viewed the same 92 images (2.9 degrees visual angle overlaid with a gray fixation cross). (a) For MEG, images were presented in random order every 1.5 – 2 s. Every 3 – 5 trials, a paper clip was presented prompting a button press response. (b) For fMRI, stimulus onset asynchrony was 3s, or 6s when a null trial (uniform gray background) was shown. During null trials the fixation cross changed to dark gray, prompting a button press response. (c) For behavioral testing, participants classified pairs of images either by identity (same/different image) or by category for 5 different categorizations: animacy, naturalness, face versus body, human versus non-human body, human versus non-human face in blocks of 24 trials each. Before every block, participants received instructions about the categorization task (e.g. animate versus inanimate). Each trial consisted of a red fixation cross (0.5 s) then two images (0.5 s, separating offset 0.5 s). Participants were instructed to respond as fast and accurately as possible, indicating whether the two images were same or different with respect to the instructed classification by pressing a button. Participants completed 8 runs, each consisting of a random sequence of the 6 blocks, given the 6 classification tasks. Results (reaction times for correct responses, and percent correct responses) were determined for each block and then averaged by participant.

Supplementary Figure 2 Linear separability of categorical subdivisions.

(a) We determined whether the membership of an image to a category (here shown for animacy) can be linearly discriminated by visual representation directly. Analysis was conducted independently for each participant and session, and for each time point from –100 to 1200 ms in 10ms steps. For each category subdivision, we subsampled the set of objects by randomly drawing M (12) objects. Each object was presented N times. We assigned (N–1) × (M–1) trials to a training set of a linearized SVM (liblinear, in the L2-regularized L2-loss SVM (primal) configuration. We tested the SVM on independent trials in two ways: from objects included in the training set ('identical' condition, dark gray), or held out from the training set ('held-out' condition, light gray). We repeated the above procedure 100 times, using different subsamples of objects and random assignment of trials to training and testing sets. Decoding accuracy was averaged across repetitions. (b–f) The upper panel shows the decoding accuracy time courses for objects included or held-out from the training set (color-coded as in (a)). The lower panel illustrates the difference of decoding accuracy between identical and held-out objects. Stars indicate time points with significant effects (sign-permutation test, n = 16, cluster-defining threshold P < 0.001, corrected significance level P < 0.05). For details see Supplementary Table 1e. Abbreviations: dec. acc. = decoding

Supplementary Figure 3 Relation of behavior to peak latency of decoding accuracy.

We determined whether (a) reaction time and (b) correctness are linearly related to peak latency of decoding accuracy (Pearson's R). We assessed significance by bootstrapping the sample of participants (n = 16, P < 0.05). Reaction time shows a positive relationship (R = 0.53, P = 0.003); correctness a negative relationship (R = –0.49, P = 0.012).

Supplementary Figure 4 Representational similarity analysis of fMRI responses in human V1 and IT.

Our analyses corroborated previous major findings3 by a random-effects analysis. (a) Representational dissimilarity matrices for human V1 and IT. Dissimilarity between fMRI pattern responses is color-coded as percentiles of dissimilarity (1– Spearman's R). (b) MDS and (c) hierarchical clustering of fMRI responses. MDS (criterion: metric stress) showed a grouping of images into inanimate objects, faces, and bodies in IT (stress = 0.24), but not in V1 (stress = 0.20). Unsupervised hierarchical clustering (criterion: average fMRI response pattern dissimilarity) revealed a nested hierarchical structure dividing animate and inanimate objects, and animates into faces and bodies in IT, but not in V1. (d) We compared dissimilarity (1 – Spearman's R) within versus between the subdivision of animate and inanimate objects. A large animacy effect was observed in IT, and a small effect in V1. A sign permutation test (n = 15, 50,000 iterations) showed that the effect was significant both in IT (P = 2e – 5) and in V1 (P = 0.0046), and significantly larger in IT (P = 2e – 5).

Supplementary Figure 5 Representational similarity analysis related MEG and fMRI responses in IT for the six subdivisions of the image set.

Representational dissimilarities were similar for all subdivisions except non-human faces. Stars above the time course indicate time points of statistical significance (sign permutation test, n = 16, cluster-defining threshold P < 0.001, corrected significance level P < 0.05). For details see Supplementary Table 1f.

Supplementary Figure 6 Representational similarity analysis related MEG and fMRI responses in human IT based on previously reported fMRI data.

MEG correlated significantly with human IT: onset at 68 ms (57 – 71 ms), peak at 158 ms (152 – 300 ms), showing reproducibility of effects across distinct data sets3. Stars above the time course indicate time points of statistical significance (sign-permutation test, n = 16, cluster-defining threshold P < 0.001, corrected significance level P < 0.05).

Supplementary Figure 7 Representational similarity analysis related MEG and fMRI for central and peripheral V1.

(a) fMRI signals in both central and peripheral V1 correlated with early MEG signals (for details see Supplementary Table 1d). (b) MEG signals correlated more strongly with fMRI signals in central than peripheral V1, demonstrating the refined spatial specificity achieved by combining MEG and fMRI by representational similarity analysis. Stars above the time course indicate time points of statistical significance (sign-permutation test, n = 16, cluster-defining threshold P < 0.001, corrected significance level P < 0.05).

Supplementary information

Supplementary Text and Figures

Supplementary Figures 1–7 and Supplementary Table 2 (PDF 3988 kb)

Supplementary Table 1

Comparison of peak latencies for discrimination of individual images at different levels of categorization. The table reports P-values determined by bootstrapping the sample of participants (50,000 samples). Significant comparisons are indexed with a star (P < 0.05, Bonferroni corrected). Latency differences between the classifications of 'Human versus non-human body' and 'Individual images' were in line with predictions, but did not pass Bonferroni correction. (XLSX 39 kb)

Decoding accuracy matrices and accompanying MDS solutions.

To allow a temporally unbiased and complete view of the MEG decoding accuracy data, we generated a movie from −100 to +1,000 ms in 1 ms steps, showing the averaged decoding accuracy across participants (n = 16) and the respective MDS solution (first two dimensions). To allow comparison of the common structure in the MDS across time, we used Procrustes alignment between the first two dimensions of the MDS solutions at neighboring time points. (AVI 8959 kb)

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Cichy, R., Pantazis, D. & Oliva, A. Resolving human object recognition in space and time. Nat Neurosci 17, 455–462 (2014).

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