Facial expressions are inherently dynamic, and our visual system is sensitive to subtle changes in their temporal sequence. However, researchers often use dynamic morphs of photographs—simplified, linear representations of motion—to study the neural correlates of dynamic face perception. To explore the brain's sensitivity to natural facial motion, we constructed a novel dynamic face database using generative neural networks, trained on a verified set of video-recorded emotional expressions. The resulting deepfakes, consciously indistinguishable from videos, enabled us to separate biological motion from photorealistic form. Results showed that conventional dynamic morphs elicit distinct responses in the brain compared to videos and photos, suggesting they violate expectations (n400) and have reduced social salience (late positive potential). This suggests that dynamic morphs misrepresent facial dynamism, resulting in misleading insights about the neural and behavioural correlates of face perception. Deepfakes and videos elicited largely similar neural responses, suggesting they could be used as a proxy for real faces in vision research, where video recordings cannot be experimentally manipulated. And yet, despite being consciously undetectable as fake, deepfakes elicited an expectation violation response in the brain. This points to a neural sensitivity to naturalistic facial motion, beyond conscious awareness. Despite some differences in neural responses, the realism and manipulability of deepfakes make them a valuable asset for research where videos are unfeasible. Using these stimuli, we proposed a novel marker for the conscious perception of naturalistic facial motion – Frontal delta activity – which was elevated for videos and deepfakes, but not for photos or dynamic morphs.

Within the last decade, Deep Artificial Neural Networks (DNNs) have emerged as powerful computer vision systems that match or exceed human performance on many benchmark tasks such as image classification. But whether current DNNs are suitable computational models of the human visual system remains an open question: While DNNs have proven to be capable of predicting neural activations in primate visual cortex, psychophysical experiments have shown behavioral differences between DNNs and human subjects, as quantified by error consistency. Error consistency is typically measured by briefly presenting natural or corrupted images to human subjects and asking them to perform an n-way classification task under time pressure. But for how long should stimuli ideally be presented to guarantee a fair comparison with DNNs? Here we investigate the influence of presentation time on error consistency, to test the hypothesis that higher-level processing drives behavioral differences. We systematically vary presentation times of backward-masked stimuli from 8.3ms to 266ms and measure human performance and reaction times on natural, lowpass-filtered and noisy images. Our experiment constitutes a fine-grained analysis of human image classification under both image corruptions and time pressure, showing that even drastically time-constrained humans who are exposed to the stimuli for only two frames, i.e. 16.6ms, can still solve our 8-way classification task with success rates way above chance. We also find that human-to-human error consistency is already stable at 16.6ms.

Visual knowledge obtained from our lifelong experience of the world plays a critical role in our ability to build short-term memories. We propose a mechanistic explanation of how working memory (WM) representations are built from the latent representations of visual knowledge and can then be reconstructed. The proposed model, Memory for Latent Representations (MLR), features a variational autoencoder with an architecture that corresponds broadly to the human visual system and an activation-based binding pool of neurons that binds items’ attributes to tokenized representations. The simulation results revealed that shape information for stimuli that the model was trained on, can be encoded and retrieved efficiently from latents in higher levels of the visual hierarchy. On the other hand, novel patterns that are completely outside the training set can be stored from a single exposure using only latents from early layers of the visual system. Moreover, the representation of a given stimulus can have multiple codes, representing specific visual features such as shape or color, in addition to categorical information. Finally, we validated our model by testing a series of predictions against behavioral results acquired from WM tasks. The model provides a compelling demonstration of visual knowledge yielding the formation of compact visual representation for efficient memory encoding.

The human visual system enables us to recognize objects (e.g., this is a cup) and act upon them (e.g., grasp the cup) with astonishing ease and accuracy. For decades, it was widely accepted that these different functions rely on two separated cortical pathways. The ventral occipitotemporal pathway subserves object recognition, while the dorsal occipitoparietal pathway promotes visually guided actions. In my talk, I will discuss recent evidence from a series of neuropsychological, developmental and neuroimaging studies that were aimed to explore the nature of object representations in the dorsal pathway. The results from these studies highlight the plausible role of the dorsal pathway in object perception and reveal an interplay between shape representations derived by the two pathways. Together, these findings challenge the binary distinction between the two pathways and are consistent with the view that object recognition is not the sole product of ventral pathway computations, but instead relies on a distributed network of regions.