Peer review process
Not revised: This Reviewed Preprint includes the authors’ original preprint (without revision), an eLife assessment, and public reviews.
Read more about eLife’s peer review process.Editors
- Reviewing EditorKristine KrugOtto-von-Guericke University Magdeburg, Magdeburg, Germany
- Senior EditorTirin MooreStanford University, Howard Hughes Medical Institute, Stanford, United States of America
Reviewer #1 (Public Review):
Summary:
This study reports that IT neurons have biased representations toward low spatial frequency (SF) and faster decoding of low SFs than high SFs. High SF-preferred neurons, and low SF-preferred neurons to a lesser degree, perform better category decoding than neurons with other profiles (U and inverted U shaped). SF coding also shows more sparseness than category coding in the earlier phase of the response and less sparseness in the later phase. The results are also contrasted with predictions of various DNN models.
Strengths:
The study addressed an important issue on the representations of SF information in a high-level visual area. Data are analyzed with LDA which can effectively reduce the dimensionality of neuronal responses and retain category information.
Weaknesses:
The results are likely compromised by improper stimulus timing and unmatched spatial frequency spectrums of stimuli in different categories.
The authors used a very brief stimulus duration (35ms), which would degrade the visual system's contrast sensitivity to medium and high SF information disproportionately (see Nachmias, JOSAA, 1967). Therefore, IT neurons in the study could have received more degraded medium and high SF inputs compared to low SF inputs, which may be at least partially responsible for higher firing rates to low Sf R1 stimuli (Figure 1c) and poorer recall performance with median and high SF R3-R5 stimuli in LDA decoding. The issue may also to some degree explain the delayed onset of recall to higher SF stimuli (Figure 2a), preferred low SF with an earlier T1 onset (Figure 2b), lower firing rate to high SF during T1 (Figure 2c), somewhat increased firing rate to high SF during T2 (because weaker high SF inputs would lead to later onset, Figure 2d).
Figure 3b shows greater face coding than object coding by high SF and to a lesser degree by low SF neurons. Only the inverted-U-shaped neurons displayed slightly better object coding than face coding. Overall the results give an impression that IT neurons are significantly more capable of coding faces than coding objects, which is inconsistent with the general understanding of the functions of IT neurons. The problem may lie with the selection of stimulus images (Figure 1b). To study SF-related category coding, the images in two categories need to have similar SF spectrums in the Fourier domain. Such efforts are not mentioned in the manuscript, and a look at the images in Figure 1b suggests that such efforts are likely not properly made. The ResNet18 decoding results in Figure 6C, in that IT neurons of different profiles show similar face and object coding, might be closer to reality.
Reviewer #2 (Public Review):
Summary:
This paper aimed to examine the spatial frequency selectivity of macaque inferotemporal (IT) neurons and its relation to category selectivity. The authors suggest in the present study that some IT neurons show a sensitivity for the spatial frequency of scrambled images. Their report suggests a shift in preferred spatial frequency during the response, from low to high spatial frequencies. This agrees with a coarse-to-fine processing strategy, which is in line with multiple studies in the early visual cortex. In addition, they report that the selectivity for faces and objects, relative to scrambled stimuli, depends on the spatial frequency tuning of the neurons.
Strengths:
Previous studies using human fMRI and psychophysics studied the contribution of different spatial frequency bands to object recognition, but as pointed out by the authors little is known about the spatial frequency selectivity of single IT neurons. This study addresses this gap and they show that at least some IT neurons show a sensitivity for spatial frequency and interestingly show a tendency for coarse-to-fine processing.
Weaknesses and requested clarifications:
1. It is unclear whether the effects described in this paper reflect a sensitivity to spatial frequency, i.e. in cycles/ deg (depends on the distance from the observer and changes when rescaling the image), or is a sensitivity to cycles /image, largely independent of image scale. How is it related to the well-documented size tolerance of IT neuron selectivity?
2. The authors' band-pass filtered phase scrambled images of faces and objects. The original images likely differed in their spatial frequency amplitude spectrum and thus it is unclear whether the differing bands contained the same power for the different scrambled images. If not, this could have contributed to the frequency sensitivity of the neurons.
3. How strong were the responses to the phase-scrambled images? Phase-scrambled images are expected to be rather ineffective stimuli for IT neurons. How can one extrapolate the effect of the spatial frequency band observed for ineffective stimuli to that for more effective stimuli, like objects or (for some neurons) faces? A distribution should be provided, of the net responses (in spikes/s) to the scrambled stimuli, and this for the early and late windows.
4. The strength of the spatial frequency selectivity is unclear from the presented data. The authors provide the result of a classification analysis, but this is in normalized units so that the reader does not know the classification score in percent correct. Unnormalized data should be provided. Also, it would be informative to provide a summary plot of the spatial frequency selectivity in spikes/s, e.g. by ranking the spatial frequency bands for each neuron based on half of the trials and then plotting the average responses for the obtained ranks for the other half of the trials. Thus, the reader can appreciate the strength of the spatial frequency selectivity, considering trial-to-trial variability. Also, a plot should be provided of the mean response to the stimuli for the two analysis windows of Figure 2c and 2d in spikes/s so one can appreciate the mean response strengths and effect size (see above).
5. It is unclear why such brief stimulus durations were employed. Will the results be similar, in particular the preference for low spatial frequencies, for longer stimulus durations that are more similar to those encountered during natural vision?
6. The authors report that the spatial frequency band classification accuracy for the population of neurons is not much higher than that of the best neuron (line 151). How does this relate to the SNC analysis, which appears to suggest that many neurons contribute to the spatial frequency selectivity of the population in a non-redundant fashion? Also, the outcome of the analyses should be provided (such as SNC and decoding (e.g. Figure 1D)) in the original units instead of undefined arbitrary units.
7. To me, the results of the analyses of Figure 3c,d, and Figure 4 appear to disagree. The latter figure shows no correlation between category and spatial frequency classification accuracies while Figure 3c,d shows the opposite.
8. If I understand correctly, the "main" test included scrambled versions of each of the "responsive" images selected based on the preceding test. Each stimulus was presented 15 times (once in each of the 15 blocks). The LDA classifier was trained to predict the 5 spatial frequency band labels and they used 70% of the trials to train the classifier. Were the trained and tested trials stratified with respect to the different scrambled images? Also, LDA assumes a normal distribution. Was this the case, especially because of the mixture of repetitions of the same scrambled stimulus and different scrambled stimuli?
9. The LDA classifiers for spatial frequency band (5 labels) and category (2 labels) have different chance and performance levels. Was this taken into account when comparing the SNC between these two classifiers? Details and SNC values should be provided in the original (percent difference) instead of arbitrary units in Figure 5a. Without such details, the results are impossible to evaluate.
10. Recording locations should be described in IT, since the latter is a large region. Did their recordings include the STS? A/P and M/L coordinate ranges of recorded neurons?
11. The authors should show in Supplementary Figures the main data for each of the two animals, to ensure the reader that both monkeys showed similar trends.
12. The authors found that the deep nets encoded better the spatial frequency bands than the IT units. However, IT units have trial-to-trial response variability and CNN units do not. Did they consider this when comparing IT and CNN classification performance? Also, the number of features differs between IT and CNN units. To me, comparing IT and CNN classification performances is like comparing apples and oranges.
13. The authors should define the separability index in their paper. Since it is the main index to show a relationship between category and spatial frequency tuning, it should be described in detail. Also, results should be provided in the original units instead of undefined arbitrary units. The tuning profiles in Figure 3A should be in spikes/s. Also, it was unclear to me whether the classification of the neurons into the different tuning profiles was based on an ANOVA assessing per neuron whether the effect of the spatial frequency band was significant (as should be done).
14. As mentioned above, the separability analysis is the main one suggesting an association between category and spatial frequency tuning. However, they compute the separability of each category with respect to the scrambled images. Since faces are a rather homogeneous category I expect that IT neurons have on average a higher separability index for faces than for the more heterogeneous category of objects, at least for neurons responsive to faces and/or objects. The higher separability for faces of the two low- and high-pass spatial frequency neurons could reflect stronger overall responses for these two classes of neurons. Was this the case? This is a critical analysis since it is essential to assess whether it is category versus responsiveness that is associated with the spatial frequency tuning. Also, I do not believe that one can make a strong claim about category selectivity when only 6 faces and 3 objects (and 6 other, variable stimuli; 15 stimuli in total) are employed to assess the responses for these categories (see next main comment). This and the above control analysis can affect the main conclusion and title of the paper.
15. For the category decoding, the authors employed intact, unscrambled stimuli. Were these from the main test? If yes, then I am concerned that this represents a too small number of stimuli to assess category selectivity. Only 9 fixed + 6 variable stimuli = 15 were in the main test. How many faces/ objects on average? Was the number of stimuli per category equated for the classification? When possible use the data of the preceding selectivity test which has many more stimuli to compute the category selectivity.