Is the face-perception system human-specific at birth?

2012 ◽  
Vol 48 (4) ◽  
pp. 1083-1090 ◽  
Author(s):  
Elisa Di Giorgio ◽  
Irene Leo ◽  
Olivier Pascalis ◽  
Francesca Simion
2012 ◽  
Vol 37 (2) ◽  
pp. 95-99 ◽  
Author(s):  
Elisa Di Giorgio ◽  
David Méary ◽  
Olivier Pascalis ◽  
Francesca Simion

The current study aimed at investigating own- vs. other-species preferences in 3-month-old infants. The infants’ eye movements were recorded during a visual preference paradigm to assess whether they show a preference for own-species faces when contrasted with other-species faces. Human and monkey faces, equated for all low-level perceptual characteristics, were used. Our results demonstrated that 3-month-old infants preferred the human face, suggesting that the face perception system becomes species-specific after 3 months of visual experience with a specific class of faces. The eye tracking results are also showing that fixations were more focused on the eye area of human faces, supporting the notion of their importance in holding visual attention.


2018 ◽  
Vol 14 (1) ◽  
pp. 81-95 ◽  
Author(s):  
Indrit Bègue ◽  
Maarten Vaessen ◽  
Jeremy Hofmeister ◽  
Marice Pereira ◽  
Sophie Schwartz ◽  
...  

2021 ◽  
Author(s):  
◽  
Ella Macaskill

<p>Face recognition is a fundamental cognitive function that is essential for social interaction – yet not everyone has it. Developmental prosopagnosia is a lifelong condition in which people have severe difficulty recognising faces but have normal intellect and no brain damage. Despite much research, the component processes of face recognition that are impaired in developmental prosopagnosia are not well understood. Two core processes are face perception, being the formation of visual representations of a currently seen face, and face memory, being the storage, maintenance, and retrieval of those representations. Most studies of developmental prosopagnosia focus on face memory deficits, but a few recent studies indicate that face perception deficits might also be important. Characterising face perception in developmental prosopagnosia is crucial for a better understanding of the condition. In this thesis, I addressed this issue in a large-scale experiment with 108 developmental prosopagnosics and 136 matched controls. I assessed face perception abilities with multiple measures and ran a broad range of analyses to establish the severity, scope, and nature of face perception deficits in developmental prosopagnosia. Three major results stand out. First, face perception deficits in developmental prosopagnosia were severe, and could be comparable in size to face memory deficits. Second, the face perception deficits were widespread, affecting the whole sample rather than a subset of individuals. Third, the deficits were mainly driven by impairments to mechanisms specialised for processing upright faces. Further analyses revealed several other features of the deficits, including the use of atypical and inconsistent strategies for perceiving faces, difficulties matching the same face across different pictures, equivalent impact of lighting and viewpoint variations in face images, and atypical perceptual and non-perceptual components of test performance. Overall, my thesis shows that face perception deficits are more central to developmental prosopagnosia than previously thought and motivates further research on the issue.</p>


NeuroImage ◽  
2009 ◽  
Vol 47 ◽  
pp. S148
Author(s):  
S Danti ◽  
C Gentili ◽  
E Ricciardi ◽  
MI Gobbini ◽  
JV Haxby ◽  
...  

Author(s):  
Shozo Tobimatsu

There are two major parallel pathways in humans: the parvocellular (P) and magnocellular (M) pathways. The former has excellent spatial resolution with color selectivity, while the latter shows excellent temporal resolution with high contrast sensitivity. Visual stimuli should be tailored to answer specific clinical and/or research questions. This chapter examines the neural mechanisms of face perception using event-related potentials (ERPs). Face stimuli of different spatial frequencies were used to investigate how low-spatial-frequency (LSF) and high-spatial-frequency (HSF) components of the face contribute to the identification and recognition of the face and facial expressions. The P100 component in the occipital area (Oz), the N170 in the posterior temporal region (T5/T6) and late components peaking at 270-390 ms (T5/T6) were analyzed. LSF enhanced P100, while N170 was augmented by HSF irrespective of facial expressions. This suggested that LSF is important for global processing of facial expressions, whereas HSF handles featural processing. There were significant amplitude differences between positive and negative LSF facial expressions in the early time windows of 270-310 ms. Subsequently, the amplitudes among negative HSF facial expressions differed significantly in the later time windows of 330–390 ms. Discrimination between positive and negative facial expressions precedes discrimination among different negative expressions in a sequential manner based on parallel visual channels. Interestingly, patients with schizophrenia showed decreased spatial frequency sensitivities for face processing. Taken together, the spatially filtered face images are useful for exploring face perception and recognition.


2017 ◽  
Vol 17 (10) ◽  
pp. 264
Author(s):  
Silvia Ubaldi ◽  
Aidas Aglinskas ◽  
Elisa Fait ◽  
Scott Fairhall

Author(s):  
Peter Thompson

Inverting the eyes and the mouth in a smiling face renders the expression grotesque. However, when this image is itself rotated through 180 degrees, the grotesque expression is no longer apparent—the smiling expression returns. This illusion, first shown with the face of the then UK prime minister Margaret Thatcher, has been explained as showing the detrimental effects of inversion on configural or holistic processing of faces. This explanation is, however, not entirely satisfactory and the illusion is still not fully understood. Variants and relevant parameters of the effect are explored, as are related concepts of inversion, expression, and face perception.


Author(s):  
Shozo Tobimatsu

There are two major parallel pathways in humans: the parvocellular (P) and magnocellular (M) pathways. The former has excellent spatial resolution with color selectivity, while the latter shows excellent temporal resolution with high contrast sensitivity. Visual stimuli should be tailored to answer specific clinical and/or research questions. This chapter examines the neural mechanisms of face perception using event-related potentials (ERPs). Face stimuli of different spatial frequencies were used to investigate how low-spatial-frequency (LSF) and high-spatial-frequency (HSF) components of the face contribute to the identification and recognition of the face and facial expressions. The P100 component in the occipital area (Oz), the N170 in the posterior temporal region (T5/T6) and late components peaking at 270-390 ms (T5/T6) were analyzed. LSF enhanced P100, while N170 was augmented by HSF irrespective of facial expressions. This suggested that LSF is important for global processing of facial expressions, whereas HSF handles featural processing. There were significant amplitude differences between positive and negative LSF facial expressions in the early time windows of 270-310 ms. Subsequently, the amplitudes among negative HSF facial expressions differed significantly in the later time windows of 330–390 ms. Discrimination between positive and negative facial expressions precedes discrimination among different negative expressions in a sequential manner based on parallel visual channels. Interestingly, patients with schizophrenia showed decreased spatial frequency sensitivities for face processing. Taken together, the spatially filtered face images are useful for exploring face perception and recognition.


1996 ◽  
Vol 8 (6) ◽  
pp. 551-565 ◽  
Author(s):  
Shlomo Bentin ◽  
Truett Allison ◽  
Aina Puce ◽  
Erik Perez ◽  
Gregory McCarthy

Event-related potentials (ERPs) associated with face perception were recorded with scalp electrodes from normal volunteers. Subjects performed a visual target detection task in which they mentally counted the number of occurrences of pictorial stimuli from a designated category such as butterflies. In separate experiments, target stimuli were embedded within a series of other stimuli including unfamiliar human faces and isolated face components, inverted faces, distorted faces, animal faces, and other nonface stimuli. Human faces evoked a negative potential at 172 msec (N170), which was absent from the ERPs elicited by other animate and inanimate nonface stimuli. N170 was largest over the posterior temporal scalp and was larger over the right than the left hemisphere. N170 was delayed when faces were presented upside-down, but its amplitude did not change. When presented in isolation, eyes elicited an N170 that was significantly larger than that elicited by whole faces, while noses and lips elicited small negative ERPs about 50 msec later than N170. Distorted human faces, in which the locations of inner face components were altered, elicited an N170 similar in amplitude to that elicited by normal faces. However, faces of animals, human hands, cars, and items of furniture did not evoke N170. N170 may reflect the operation of a neural mechanism tuned to detect (as opposed to identify) human faces, similar to the “structural encoder” suggested by Bruce and Young (1986). A similar function has been proposed for the face-selective N200 ERP recorded from the middle fusiform and posterior inferior temporal gyri using subdural electrodes in humans (Allison, McCarthy, Nobre, Puce, & Belger, 1994c). However, the differential sensitivity of N170 to eyes in isolation suggests that N170 may reflect the activation of an eye-sensitive region of cortex. The voltage distribution of N170 over the scalp is consistent with a neural generator located in the occipitotemporal sulcus lateral to the fusiform/inferior temporal region that generates N200.


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