Face superiority effect

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In psychology, the face superiority effect refers to the phenomena of how all individuals perceive and encode other human faces in memory. Rather than perceiving and encoding single features of a face (nose, eyes, mouth, etc.), we perceive and encode a human face as one holistic unified element.[1] This phenomenon aids our visual system in the recognition of thousands of faces,[2] a task that would be difficult if it were necessary to recognize sets of individual features and characteristics.[3] However, this effect is limited to perceiving upright faces and does not occur when a face is at an unusual angle, such as when faces are upside-down or contorted in phenomena like the Thatcher effect and Pareidolia.[4]

Early history

In 1879, Galton's research[5] was some of the first to indicate that the face is “the sum of a multitude of small details, which are viewed in such rapid succession that we seem to perceive them all at a single glance.” This innate “holistic” perception is one of the main factors that differentiates face recognition from object recognition. To test this and further face superiority research in general, Tanaka and Farah[6] conducted a study where they assessed individuals’ ability to recognize facial features holistically. Participants were given an allotment of time to study several faces and then were tested on their ability to recognize one feature of the face. As the researchers predicted, participants were better able to recognize the feature when it was presented with the whole face, rather than when it was presented in isolation.

Other studies confirming the holistic processing theory involve the inversion condition, similar to the Thatcher Effect, where inverted, distorted, or disoriented faces are not as easily recognized. Yin's 1969 research[7] demonstrated this and supported his hypothesis which stated that familiar faces would not be recognized if the face is presented at an inverted state. While most objects in general are difficult to recognize when inverted, Yin exhibited that inverted faces caused a particular impairment in recognition. Similarly, the Thatcher Effect presents a face that is both distorted and upside-down, which individuals typically can't detect until they are presented the same image right-side-up, and are then able to see the obvious contortions.

Neuroscience behind face superiority

Evidence from neurophysiology studies with humans and monkeys also support face superiority. Neuroimaging and electrophysiological studies in humans shows the effects of holistic face recognition. In particular, when humans are shown normal upright faces, neuroimaging displays higher brain activity and response rates in the middle fusiform gyrus (MFG), and the inferior occipital gyrus (IOG) than when shown scrambled[8] or inverted faces.[9] Additionally, experiments computing event-related scalp potentials (ERPs) reveal higher brain responses 180ms after presenting the normal face, than in inverted/scrambled conditions.[10]

Additionally, research from Riesenhuber, Jarudi, Gilad, & Sinha, 2004;[11] K. Tanaka, Saito, Fukada, & Moriya, 1991;[12] and K. Tanaka, 1996[13] also supports face superiority, where they demonstrate that face parts and wholes are similar to other hierarchical visual processes, in that the stimulation of simple features leads to the stimulation of complex features. This “feed-forward” theory states that the part-face information precedes and leads into the whole-face perception. However, the reverse model of this hierarchy states that the perception of the whole face leads to the perception of the parts.[14][15]

Prosopagnosia face blindness

Prosopagnosia is a "selective impairment in the ability to recognize individual faces due to brain damage of the visual cortex."[16] Essentially, this neurological deficit impairs an individuals ability to recognize faces, even faces of those who should be familiar, such as family members. This is the result of damage to the visual cortex. In terms of the holistic view, the inability to recognize faces stems from a failure to integrate the individual face parts into a whole.[17] A study done by Busigny, Joubert, Felician, Ceccaldi, & Rossion (2010)[17] looked at a prosopagnosia patient, GG, in reference to unimpaired control participants in matching/recognition tasks. Participants were either asked to study a whole face and select a part from the studied face presented in isolation, or study an isolated part and then select the same part when presented in a whole face. The researchers hypothesized that holistic interference would be demonstrated in the "part-to-whole" and "whole-to-part" conditions relative to the "part-to-part" and "whole-to-whole" conditions. These results were confirmed in the control participants, however, patient GG performed equally well in both conditions. The researchers suggest this is due to her recognition of face parts is unaffected by surrounding facial features in encoding or retrieving it from memory. Similar studies have also been conducted to show that prosopagnosia results from an individual's inability to form a holistic facial representation.[16]

Sequential lineup superiority effect

In criminology, the sequential lineup superiority effect refers to the process presented to eye-witnesses during criminal investigations that has to do with suspect "line ups". This can include the use of photographs of multiple individuals including a suspect (or absent of one), or a line up with living members in an effort to identify a suspect of a crime.[18] It is used mainly to assist eye-witnesses more accurately decide on an individual within the line up who most represents the suspects description. The Sequential Lineup process includes a system that shows only one suspect (photograph or live person) at a time, and forcing a decision from the witness viewing the lineup.[18] According to the research done by Steblay, Nancy, Dysart, Jennifer, and Wells, Gary L., there were fewer incidents of false identifications when the Sequential Lineup method was used.[18]

References

  1. Tanaka, J. W., & Farah, M. J. (2003). The holistic representation of faces. In M. A. Peterson, G. Rhodes, M. A. Peterson, G. Rhodes (Eds.) , Perception of faces, objects, and scenes: Analytic and holistic processes (pp. 53-71). New York, NY, US: Oxford University Press.
  2. Rhodes, G. (2013). Face recognition. In D. Reisberg, D. Reisberg (Eds.) , The Oxford handbook of cognitive psychology (pp. 46–68). New York, NY, US: Oxford University Press. doi:10.1093/oxfordhb/9780195376746.013.0004
  3. Peterson, M. A., & Rhodes, G. (2003). Perception of faces, objects, and scenes: Analytic and holistic processes. New York, NY, US: Oxford University Press.
  4. McKone, E. (2010). Face and object recognition: How do they differ?. In V. Coltheart, V. Coltheart (Eds.) , Tutorials in visual cognition (pp. 261–303). New York, NY, US: Psychology Press.
  5. Galton F. Composite portraits, made by combining those of many different persons into a single, resultant figure. Journal of the Anthropological Institute. 1879;8:132–144.
  6. Tanaka JW, Farah MJ. Parts and Wholes in Face Recognition. Quarterly Journal of Experimental Psychology. 1993;46A(2):225–245.
  7. Yin RK. Looking at upside-down faces. Journal of Experimental Psychology: General. 1969;81:141–145.
  8. Kanwisher N, McDermott J, Chun MM. The fusiform face area: a module in human extrastriate cortex specialized for face perception. Journal of Neuroscience. 1997;17:4302–4311.
  9. Yovel G, Kanwisher N. Face perception: Domain specific, not process specific. Neuron. 2004;44(5):889–898.
  10. Rossion B, Gauthier I, Tarr MJ, Despland P, Bruyer R, Linotte S, Crommelinck M. The N170 occipito-temporal component is delayed and enhanced to inverted faces but not to inverted objects: an electrophysiological account of face-specific processes in the human brain. NeuroReport. 2000;11(1):69–74.
  11. Riesenhuber M, Jarudi I, Gilad S, Sinha P. Face processing in humans is compatible with a simple shape-based model of vision. Proceedings of the Royal Society B: Biological Sciences. 2004;271(Suppl_6):S448–S450.
  12. Tanaka K, Saito H, Fukada Y, Moriya M. Coding visual images of objects in the inferotemporal cortex of the macaque monkey. Journal of Neurophysiology. 1991;66(1):170–189
  13. Tanaka K. Inferotemporal cortex and object vision. Annual Review of Neuroscience. 1996;19:109–139. doi:10.1146/annurev.neuro.19.1.109.
  14. Ahissar M, Hochetein S. Perceptual learning. In: Walsh V, Kulikowski J, editors. Perceptual constancies: Why things look as they. Cambridge University Press; Cambridge, England: 1998. pp. 455–498
  15. Hochstein S, Ahissar M. View from the top: Hierarchies and reverse hierarchies in the visual system. Neuron. 2002;36(5):791–804.
  16. 16.0 16.1 Tanaka, J. W., & Simonyi, D. (2016). The “parts and wholes” of face recognition: a review of the literature. Quarterly Journal of Experimental Psychology (2006), 69(10), 1876–1889. http://doi.org/10.1080/17470218.2016.1146780
  17. 17.0 17.1 Busigny T, Joubert S, Felician O, Ceccaldi M, Rossion B. Holistic perception of the individual face is specific and necessary: evidence from an extensive case study of acquired prosopagnosia. Neuropsychologia. 2010;48(14):4057–92.
  18. 18.0 18.1 18.2 Steblay, N. K., Dysart, J. E., & Wells, G. L. (2011). Seventy-two tests of the sequential lineup superiority effect: A meta-analysis and policy discussion. Psychology, Public Policy, And Law, 17(1), 99-139. doi:10.1037/a0021650